17401-06-8((-)-1,4-DI-O-BENZYL-L-THREITOL)
Product Description
17401-06-8
CAS No.
17401-06-8
Chemical Name:
(-)-1,4-DI-O-BENZYL-L-THREITOL
CBNumber:
CB1144985
Molecular Formula:
C18H22O4
Formula Weight:
302.36
MOL File:
Mol file
(-)-1,4-DI-O-BENZYL-L-THREITOL Synonyms:
(-)-1,4-DI-O-BENZYL-L-THREITOL
1,4-DI-O-BENZYL-L-THREITOL
(-)-1,4-DI-O-BENZYL-L-THREITOL 98+%
(-)-(2S,3S)-1,4-BIS(BENZYLOXY)-2,3-BUTANEDIOL
(2S,3S)-(-)-1,4-DIBENZYLOXY-2,3-BUTANEDIOL
(S,S)-1,4-Di-O-benzyl-D-threitol
2,3-BUTANEDIOL, 1,4-BIS(PHENYLMETHOXY)-, (2S,3S)-
(-)-1,4-Di-O-benzyl-L-threitol, 1,4-Di-O-benzyl-L-threitol, (-)-(2S,3S)-1,4-Bis(benzyloxy)-2,3-butanediol
(-)-1,4-DI-O-BENZYL-L-THREITOL
Property
Melting point:
55-58 °C
Boiling point:
484.4±45.0 °C(Predicted)
Density
1.174±0.06 g/cm3(Predicted)
refractive index
-6.3 ° (C=5, CHCl3)
storage temp.
2-8°C
solubility
almost transparency in Chloroform
form
powder to crystal
pka
13.24±0.20(Predicted)
color
White to Almost white
optical activity
[α]20/D 6°, c = 5 in chloroform
BRN
2149394
CAS DataBase Reference
17401-06-8(CAS DataBase Reference)
Safety
WGK Germany :
3
HS Code :
2909.49.1500
(-)-1,4-DI-O-BENZYL-L-THREITOL
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17401-06-8((-)-1,4-DI-O-BENZYL-L-THREITOL)
Related Search:
(-)-1,4-DI-O-BENZYL-L-THREITOL
1,4-DI-O-BENZYL-L-THREITOL
(-)-1,4-DI-O-BENZYL-L-THREITOL 98+%
(-)-(2S,3S)-1,4-BIS(BENZYLOXY)-2,3-BUTANEDIOL
(2S,3S)-(-)-1,4-DIBENZYLOXY-2,3-BUTANEDIOL
(S,S)-1,4-Di-O-benzyl-D-threitol
2,3-BUTANEDIOL, 1,4-BIS(PHENYLMETHOXY)-, (2S,3S)-
(-)-1,4-Di-O-benzyl-L-threitol, 1,4-Di-O-benzyl-L-threitol, (-)-(2S,3S)-1,4-Bis(benzyloxy)-2,3-butanediol
1-O,4-O-Dibenzyl-L-threitol
(-)-1,4-Di-O-benzylthreitol
(S,S)-1,4-Bis(benzyloxy)-2,3-butanediol
1,4-bis(phenylmethoxy)butane-2,3-diol
(-)-1,4-Di-O-benzyl-L-threitol>
(-)-1,4-Di-O-benzyl-L-threitol
17401-06-8
C6H5CH2OCH2CHOH2
Monosaccharides
Specialty Synthesis
Sugar Alcohols
Simple Alcohols (Chiral)
Chiral Building Blocks
Asymmetric Synthesis
Sugars
Carbohydrate Synthesis
Asymmetric Synthesis
Biochemistry
Chiral Building Blocks
Simple Alcohols (Chiral)
Sugar Alcohols
Sugars
Synthetic Organic Chemistry
chiral
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