Cas 949570-30-3,4-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-2(E)-buten-1-ol

949570-30-3

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Basic information

Product Name: 4-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-2(E)-buten-1-ol
Synonyms: 4-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-2(E)-buten-1-ol
CAS NO:949570-30-3
Molecular Formula:
Molecular Weight: 594.748
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-2(E)-buten-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: 4-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-2(E)-buten-1-ol(949570-30-3)
EPA Substance Registry System: 4-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-2(E)-buten-1-ol(949570-30-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 949570-30-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 949570-30-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,9,5,7 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 949570-30:
(8*9)+(7*4)+(6*9)+(5*5)+(4*7)+(3*0)+(2*3)+(1*0)=213
213 % 10 = 3
So 949570-30-3 is a valid CAS Registry Number.

949570-30-3Upstream product

949570-29-0 ethyl 4-(2',3',4',6'-tetra-O-benzyl-α-D-galactopyranosyl)-2(E)-butenoate

949570-30-3Downstream Products

949570-30-3Relevant academic research and scientific papers

An improved two-step synthetic route to primary allylic alcohols from aldehydes

Liu, Zheng,Gong, Yaqiong,Byun, Hoe-Sup,Bittman, Robert

experimental part, p. 470 - 475 (2010/06/14)

An improved two-step synthetic route to allylic alcohols from aldehydes has been developed. A modification of the HWE reaction in H2O-2-PrOH (1 : 1) and a convenient protocol to prepare AlH3 in THF from LiAlH 4 and n-BuBr are the key factors in the improvement.

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