Cas 1198587-45-9,methyl 2-O-benzyl-3-C-nitromethyl-4-(4-methylphenyl)sulfonyl-6-O-triphenylmethyl-α-D-glucopyranoside

1198587-45-9

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Basic information

Product Name: methyl 2-O-benzyl-3-C-nitromethyl-4-(4-methylphenyl)sulfonyl-6-O-triphenylmethyl-α-D-glucopyranoside
Synonyms: methyl 2-O-benzyl-3-C-nitromethyl-4-(4-methylphenyl)sulfonyl-6-O-triphenylmethyl-α-D-glucopyranoside
CAS NO:1198587-45-9
Molecular Formula:
Molecular Weight: 707.844
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 2-O-benzyl-3-C-nitromethyl-4-(4-methylphenyl)sulfonyl-6-O-triphenylmethyl-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-O-benzyl-3-C-nitromethyl-4-(4-methylphenyl)sulfonyl-6-O-triphenylmethyl-α-D-glucopyranoside(1198587-45-9)
EPA Substance Registry System: methyl 2-O-benzyl-3-C-nitromethyl-4-(4-methylphenyl)sulfonyl-6-O-triphenylmethyl-α-D-glucopyranoside(1198587-45-9)

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: 1198587-45-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1198587-45-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,5,8 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1198587-45:
(9*1)+(8*1)+(7*9)+(6*8)+(5*5)+(4*8)+(3*7)+(2*4)+(1*5)=219
219 % 10 = 9
So 1198587-45-9 is a valid CAS Registry Number.

1198587-45-9Upstream product

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1198587-45-9Relevant academic research and scientific papers

Vinyl sulfone modified hex-3-enopyranosides: novel routes to C3-C4 and C4-C5 cyclopropanated pyranosides

Bhattacharya, Rahul,Dey, Debanjana,Pathak, Tanmaya

experimental part, p. 5255 - 5260 (2010/01/18)

In a departure from metal-based cyclopropanation reactions, 4-sulfon.ylhex-3-ernopyranosides carrying a leaving group at either of the two γ-positions are used as efficient intermediates for the synthesis of C3-C4 and C4-C5 cyclopropanated pyranosides.

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