(+)-2,3-O-Isopropylidene-L-threitol

  • CasNo:50622-09-8
  • purity:99%
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Quality products?make an important contribution to long-term revenue and profitability. (+)-2,3-O-Isopropylidene-L-threitol GMP Manufacturer Global Trade 50622-09-8 with Fast Delivery

1.What is the (+)-2,3-O-Isopropylidene-L-threitol ?

(+)-2,3-O-Isopropylidene-L-threitol is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuff.

(-)-dimethy-2,3-O-isopropylidene-L-tartrate
37031-29-1

(-)-dimethy-2,3-O-isopropylidene-L-tartrate

2,3-O-isopropylidene-L-threitol
50622-09-8

2,3-O-isopropylidene-L-threitol

Conditions
Conditions Yield
With methanol; sodium tetrahydroborate;
100%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 2h; Inert atmosphere; Reflux; Schlenk technique;
98%
With methanol; sodium tetrahydroborate; at 0 - 20 ℃; for 0.5h;
98%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 20 ℃;
96%
With lithium aluminium tetrahydride; In tetrahydrofuran; for 0.5h; Heating;
94%
With sodium tetrahydroborate; In methanol; at 0 ℃; for 1h; Inert atmosphere;
93%
With sodium tetrahydroborate; In methanol; at 0 ℃;
92%
With lithium aluminium tetrahydride; In diethyl ether; for 5h; Heating;
92%
With sodium tetrahydroborate; In methanol; at 0 ℃; for 0.5h;
92%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 16h; optical yield given as %de; Reflux; Inert atmosphere;
91%
With lithium aluminium tetrahydride;
90%
With lithium aluminium tetrahydride; for 6h; Reflux;
90%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 70 ℃; for 2.25h;
89%
With lithium aluminium tetrahydride; In tetrahydrofuran;
88%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 20 ℃; for 48h; Cooling with ice;
88%
With lithium aluminium tetrahydride; In tetrahydrofuran; for 3h; Heating;
85%
With sodium tetrahydroborate; In methanol; at 0 - 20 ℃; Inert atmosphere;
84%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃;
83%
With lithium aluminium tetrahydride; In tetrahydrofuran;
82%
With lithium aluminium tetrahydride; In tetrahydrofuran; Reflux;
82%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 0.5h; Reflux;
82%
With sodium tetrahydroborate; In methanol;
80%
(-)-dimethy-2,3-O-isopropylidene-L-tartrate; With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 1.25h; Inert atmosphere;
With water; sodium hydroxide; In tetrahydrofuran; for 0.166667h;
80%
With lithium aluminium tetrahydride; In tetrahydrofuran; for 4h; Heating;
77%
With lithium aluminium tetrahydride; In tetrahydrofuran; for 3h; Reflux; Inert atmosphere;
75%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 3h; Reflux;
72%
With lithium aluminium tetrahydride; In diethyl ether; at -10 - 20 ℃; for 4h;
70%
With sodium tetrahydroborate; In methanol; at 0 - 20 ℃;
67%
With sodium tetrahydroborate; In ethanol; at -20 - 20 ℃;
61%
With lithium aluminium tetrahydride;
59%
With lithium aluminium tetrahydride; In diethyl ether; for 3h; Heating;
59%
With lithium aluminium tetrahydride; In diethyl ether; Ambient temperature;
45%
With lithium aluminium tetrahydride; In diethyl ether; Heating;
With lithium aluminium tetrahydride;
With lithium aluminium tetrahydride; In tetrahydrofuran; for 26h; Heating;
With sodium tetrahydroborate; In methanol; at 20 ℃; for 4h; Cooling with ice; Inert atmosphere;
(-)-dimethy-2,3-O-isopropylidene-L-tartrate; With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 26.5h; Heating / reflux;
With sodium hydroxide; water; In tetrahydrofuran; at 20 ℃; for 5.42h;
With lithium aluminium tetrahydride; In tetrahydrofuran; for 16h; Reflux;
7 g
With sodium tetrahydroborate; In methanol; at 0 - 20 ℃; for 2h;
With lithium aluminium tetrahydride; In diethyl ether; at 0 - 20 ℃; for 1.25h;
650.2 mg
With sodium tetrahydroborate; In methanol; at 20 ℃; for 4h; Inert atmosphere;
diethyl (4R,5R)-2,2-dimethyl-1,3-dioxolane-4,5-dicarboxylate
59779-75-8

diethyl (4R,5R)-2,2-dimethyl-1,3-dioxolane-4,5-dicarboxylate

2,3-O-isopropylidene-L-threitol
50622-09-8

2,3-O-isopropylidene-L-threitol

Conditions
Conditions Yield
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 65 ℃; for 7h;
98%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 40 ℃; for 5.5h;
95%
diethyl (4R,5R)-2,2-dimethyl-1,3-dioxolane-4,5-dicarboxylate; With lithium aluminium tetrahydride; In tetrahydrofuran; Cooling with ice; Reflux;
With sodium hydroxide; In tetrahydrofuran; water; ethyl acetate; at 0 ℃;
95%
diethyl (4R,5R)-2,2-dimethyl-1,3-dioxolane-4,5-dicarboxylate; With lithium aluminium tetrahydride; In tetrahydrofuran; at 23 ℃; for 1h;
With sodium hydroxide; water; for 1.5h; Further stages.;
94%
With sodium bis(2-methoxyethoxy)aluminium dihydride; In diethyl ether; toluene; at 20 ℃; for 3h;
90%
With lithium aluminium tetrahydride; In diethyl ether; at 20 ℃; for 14h; Inert atmosphere;
89%
With lithium aluminium tetrahydride; In diethyl ether; at 20 ℃; for 14h; Inert atmosphere;
89%
With sodium tetrahydroborate; lithium chloride; In tetrahydrofuran; ethanol; at 20 ℃; for 20h;
86%
With lithium aluminium tetrahydride;
85%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 2h;
85%
With lithium aluminium tetrahydride; In diethyl ether;
84%
With lithium aluminium tetrahydride; In diethyl ether; at 36 ℃; for 3h;
84%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 45 ℃; for 5.5h;
83%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 45 ℃; for 5.5h;
83%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 ℃; for 5h; Inert atmosphere; Reflux;
81%
With sodium tetrahydroborate; In tetrahydrofuran; at 70 ℃; for 4h;
78%
With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 20 ℃;
78%
With lithium aluminium tetrahydride; In diethyl ether; for 16h; Heating;
77%
With sodium tetrahydroborate; lithium chloride;
76%
With sodium tetrahydroborate; In ethanol; at 0 ℃; for 6h;
69%
With sodium tetrahydroborate;
65%
With lithium aluminium tetrahydride;
62%
With lithium aluminium tetrahydride; In tetrahydrofuran; Heating;
47%
With sodium tetrahydroborate; In ethanol; Heating; 150-210 min.;
With lithium aluminium tetrahydride;
With lithium aluminium tetrahydride;
With lithium aluminium tetrahydride; In tetrahydrofuran; for 5h; Heating;
With lithium aluminium tetrahydride; In tetrahydrofuran; for 4h; Heating;
18.9 g
With lithium aluminium tetrahydride; In tetrahydrofuran;
With lithium aluminium tetrahydride; In tetrahydrofuran;
With lithium aluminium tetrahydride; In tetrahydrofuran;
With lithium aluminium tetrahydride; In tetrahydrofuran; at 70 ℃; for 1h;
2.2 g
With lithium aluminium tetrahydride; In tetrahydrofuran; diethyl ether; Schlenk technique; Inert atmosphere;
With sodium tetrahydroborate; lithium chloride; In tetrahydrofuran; ethanol; at 0 - 40 ℃; for 18h; Inert atmosphere;
14 g

2.What is the CAS number for (+)-2,3-O-Isopropylidene-L-threitol ?

The CAS number of (+)-2,3-O-Isopropylidene-L-threitol is 50622-09-8.

More information of (+)-2,3-O-Isopropylidene-L-threitol 50622-09-8 are:

CAS?Number

50622-09-8

Density

1.108 g/cm3

Melting Point

46-50 °C

Boiling Point

335.9 °C at 760 mmHg

Flash Point

111.9 °C

Vapor Pressure

8.03E-06mmHg at 25°C

Refractive Index

3.9 ° (C=5, Acetone)

HS CODE

29329970

PSA

58.92000

LogP

-0.50890

Pka

13.90±0.10(Predicted)

3.What are another words for (+)-2,3-O-Isopropylidene-L-threitol ?

Synonyms?for?(+)-2,3-O-Isopropylidene-L-threitol 50622-09-8:1,3-Dioxolane-4,5-dimethanol,2,2-dimethyl-, (4S-trans)-;(+)-2,3-O-Isopropylidene-L-threitol;(4S,5S)-4,5-Bis(hydroxymethyl)-2,2-dimethyl-1,3-dioxolane;2,3-O-Isopropylidene-L-threitol;

4.What is the molecular formula of (+)-2,3-O-Isopropylidene-L-threitol?

The chemical formula of ?(+)-2,3-O-Isopropylidene-L-threitol is?C7H14O4 which containing 7 Carbon atoms,14 Hydrogen atoms and 4 Oxygen atoms,and the molecular weight of??(+)-2,3-O-Isopropylidene-L-threitol?is 162.186.

5.What is (+)-2,3-O-Isopropylidene-L-threitol (50622-09-8) used for?

(+)-2,3-O-Isopropylidene-L-threitol is a significant organic compound characterized by its white transparent, adhering, needle-like crystalline structure. It serves as a crucial raw material and intermediate in various industries due to its unique chemical properties and reactivity.

InChI:InChI=1/C7H14O4/c1-7(2)10-5(3-8)6(4-9)11-7/h5-6,8-9H,3-4H2,1-2H3/t5-,6-/m0/s1

Relevant articles related to (+)-2,3-O-Isopropylidene-L-threitol:

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