Cas 1407488-40-7,O-(3,4,6-tri-O-benzyl-2-deoxy-α-D-galactopyranosyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-serine allyl ester

1407488-40-7

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Basic information

Product Name: O-(3,4,6-tri-O-benzyl-2-deoxy-α-D-galactopyranosyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-serine allyl ester
Synonyms:
CAS NO:1407488-40-7
Molecular Formula:
Molecular Weight: 783.918
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: O-(3,4,6-tri-O-benzyl-2-deoxy-α-D-galactopyranosyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-serine allyl ester(CAS DataBase Reference)
NIST Chemistry Reference: O-(3,4,6-tri-O-benzyl-2-deoxy-α-D-galactopyranosyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-serine allyl ester(1407488-40-7)
EPA Substance Registry System: O-(3,4,6-tri-O-benzyl-2-deoxy-α-D-galactopyranosyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-serine allyl ester(1407488-40-7)

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: 1407488-40-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1407488-40-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,7,4,8 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1407488-40:
(9*1)+(8*4)+(7*0)+(6*7)+(5*4)+(4*8)+(3*8)+(2*4)+(1*0)=167
167 % 10 = 7
So 1407488-40-7 is a valid CAS Registry Number.

1407488-40-7Upstream product

136497-85-3 N-(9-fluorenylmethoxycarbonyl)-L-serine allyl ester

1407488-40-7Downstream Products

1407488-40-7Relevant academic research and scientific papers

Halide effects on cyclopropenium cation promoted glycosylation with deoxy sugars: Highly α-selective glycosylations using a 3,3-dibromo-1,2- diphenylcyclopropene promoter

Nogueira, Jason M.,Issa, John Paul,Chu, An-Hsiang Adam,Sisel, Jordan A.,Schum, Ryan S.,Bennett, Clay S.

supporting information, p. 4927 - 4930 (2012/11/13)

A mixture of 3,3-dibromocyclopropene and TBAI promotes highly α-selective glycosylation reactions (up to >20:1) by using deoxy sugar hemiacetal donors. The reaction provides a convenient method for generating highly reactive glycosyl donors in situ from s

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