Cas 130781-47-4,methyl 4-O-benzoyl-6-bromo-2-(carboxymethyl)-2,6-dideoxy-α-D-allopyranoside-γ-lactone

130781-47-4

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Basic information

Product Name: methyl 4-O-benzoyl-6-bromo-2-(carboxymethyl)-2,6-dideoxy-α-D-allopyranoside-γ-lactone
Synonyms: methyl 4-O-benzoyl-6-bromo-2-(carboxymethyl)-2,6-dideoxy-α-D-allopyranoside-γ-lactone
CAS NO:130781-47-4
Molecular Formula:
Molecular Weight: 385.211
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: methyl 4-O-benzoyl-6-bromo-2-(carboxymethyl)-2,6-dideoxy-α-D-allopyranoside-γ-lactone(CAS DataBase Reference)
NIST Chemistry Reference: methyl 4-O-benzoyl-6-bromo-2-(carboxymethyl)-2,6-dideoxy-α-D-allopyranoside-γ-lactone(130781-47-4)
EPA Substance Registry System: methyl 4-O-benzoyl-6-bromo-2-(carboxymethyl)-2,6-dideoxy-α-D-allopyranoside-γ-lactone(130781-47-4)

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: 130781-47-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 130781-47-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,7,8 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 130781-47:
(8*1)+(7*3)+(6*0)+(5*7)+(4*8)+(3*1)+(2*4)+(1*7)=114
114 % 10 = 4
So 130781-47-4 is a valid CAS Registry Number.

130781-47-4Upstream product

130781-46-3 (4aR,6S,6aR,9aS,9bS)-6-Methoxy-2-phenyl-hexahydro-furo[2',3':4,5]pyrano[3,2-d][1,3]dioxin-8-one

130781-47-4Downstream Products

130781-47-4Relevant academic research and scientific papers

An Improved Procedure for the Ring Opening of Benzylidene Acetals with N-Bromosuccinimide

Chretien, Francoise,Khaldi, Mustapha,Chapleur, Yves

, p. 1589 - 1596 (2007/10/02)

A new procedure for the ring opening of 4,6-O-benzylidene acetals of carbohydrates with N-bromosuccinimide using calcium carbonate in stoechiometric amount instead of excess barium carbonate is described.This procedure is succesfully applied to some highl

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