Cas 114643-52-6,tert-butyl p-<4-azido-2-(tert-butoxycarbonyl)amino-2,4-dideoxy-6-O-tolylsulfonyl-α-D-glucopyranosyloxy>cinnamate

114643-52-6

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Basic information

Product Name: tert-butyl p-<4-azido-2-(tert-butoxycarbonyl)amino-2,4-dideoxy-6-O-tolylsulfonyl-α-D-glucopyranosyloxy>cinnamate
Synonyms: tert-butyl p-<4-azido-2-(tert-butoxycarbonyl)amino-2,4-dideoxy-6-O-tolylsulfonyl-α-D-glucopyranosyloxy>cinnamate
CAS NO:114643-52-6
Molecular Formula:
Molecular Weight: 660.745
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: tert-butyl p-<4-azido-2-(tert-butoxycarbonyl)amino-2,4-dideoxy-6-O-tolylsulfonyl-α-D-glucopyranosyloxy>cinnamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl p-<4-azido-2-(tert-butoxycarbonyl)amino-2,4-dideoxy-6-O-tolylsulfonyl-α-D-glucopyranosyloxy>cinnamate(114643-52-6)
EPA Substance Registry System: tert-butyl p-<4-azido-2-(tert-butoxycarbonyl)amino-2,4-dideoxy-6-O-tolylsulfonyl-α-D-glucopyranosyloxy>cinnamate(114643-52-6)

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: 114643-52-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114643-52-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,6,4 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 114643-52:
(8*1)+(7*1)+(6*4)+(5*6)+(4*4)+(3*3)+(2*5)+(1*2)=106
106 % 10 = 6
So 114643-52-6 is a valid CAS Registry Number.

114643-52-6Upstream product

114643-52-6Downstream Products

114643-52-6Relevant academic research and scientific papers

SYNTHESIS OF N1-(p-GLYCOSYLOXYCINNAMOYL)SPERMIDINES

Saito, Yoshihiro,Watanabe, Tsuyoshi,Hashimoto, Hironobu,Yoshimura, Juji

, p. 171 - 188 (1987)

The synthesis of O-glycosylated N1-(p-hydroxycinnamoyl)spermidines was investigated. p-Hydroxycinnamate glycosides of some amino sugars, including a synthetic intermediate of a unique antibiotic, cinodine, were prepared and converted into the amide of spermidine.

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