Cas 1315192-47-2,allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside

1315192-47-2

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Basic information

Product Name: allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside
Synonyms: allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside
CAS NO:1315192-47-2
Molecular Formula:
Molecular Weight: 710.865
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: allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside(1315192-47-2)
EPA Substance Registry System: allyl 2,4-di-O-benzyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-benzyl-α-L-rhamnopyranoside(1315192-47-2)

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: 1315192-47-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1315192-47-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,1,9 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1315192-47:
(9*1)+(8*3)+(7*1)+(6*5)+(5*1)+(4*9)+(3*2)+(2*4)+(1*7)=132
132 % 10 = 2
So 1315192-47-2 is a valid CAS Registry Number.

1315192-47-2Upstream product

1315192-47-2Downstream Products

1315192-55-2 C₇₇H₈₉N₃O₁₆

1315192-47-2Relevant academic research and scientific papers

Concise synthesis of Bacillus anthracis exosporium tetrasaccharide via two-stage activation of allyl glycosyl donor strategy

Wang, Yun,Liang, Xing,Wang, Pengfei

supporting information; experimental part, p. 3912 - 3915 (2011/08/09)

A highly efficient glycosylation protocol recently developed in our laboratory has been utilized in the short synthesis of the tetrasaccharide 1, an antigen important to the development of carbohydrate-based diagnostic tools and vaccines against anthrax.

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