Cas 185801-19-8,methyl 3,4-di-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside

185801-19-8

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Basic information

Product Name: methyl 3,4-di-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside
Synonyms: methyl 3,4-di-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside
CAS NO:185801-19-8
Molecular Formula:
Molecular Weight: 507.584
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 3,4-di-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 3,4-di-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside(185801-19-8)
EPA Substance Registry System: methyl 3,4-di-O-benzyl-2-benzyloxycarbonylamino-2-deoxy-α-D-glucopyranoside(185801-19-8)

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: 185801-19-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 185801-19-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,8,0 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 185801-19:
(8*1)+(7*8)+(6*5)+(5*8)+(4*0)+(3*1)+(2*1)+(1*9)=148
148 % 10 = 8
So 185801-19-8 is a valid CAS Registry Number.

185801-19-8Upstream product

93000-11-4 methyl 3-O-benzyl-4,6-O-benzylidene-2-(benzyloxycarbonyl)amino-2-deoxy-α-D-glucopyranoside

185801-19-8Downstream Products

185801-19-8Relevant academic research and scientific papers

Regio- and chemoselective reductive cleavage of 4,6-O-benzylidene-type acetals of hexopyranosides using BH3·THF-TMSOTf

Daragics, Katalin,Fügedi, Péter

experimental part, p. 2914 - 2916 (2009/09/06)

Benzylidene-type cyclic acetals of carbohydrates undergo efficient reductive ring opening using BH3·THF and a catalytic amount of TMSOTf at room temperature. 4,6-O-Benzylidene-hexopyranosides afford the corresponding 4-O-benzyl ethers exclusive

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