Cas 136409-47-7,(3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-carboxylic acid 2-thioxo-2H-pyridin-1-yl ester

136409-47-7

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Basic information

Product Name: (3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-carboxylic acid 2-thioxo-2H-pyridin-1-yl ester
Synonyms: (3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-carboxylic acid 2-thioxo-2H-pyridin-1-yl ester
CAS NO:136409-47-7
Molecular Formula:
Molecular Weight: 557.667
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: (3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-carboxylic acid 2-thioxo-2H-pyridin-1-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-carboxylic acid 2-thioxo-2H-pyridin-1-yl ester(136409-47-7)
EPA Substance Registry System: (3R,4R,5R)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-carboxylic acid 2-thioxo-2H-pyridin-1-yl ester(136409-47-7)

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: 136409-47-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 136409-47-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,4,0 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 136409-47:
(8*1)+(7*3)+(6*6)+(5*4)+(4*0)+(3*9)+(2*4)+(1*7)=127
127 % 10 = 7
So 136409-47-7 is a valid CAS Registry Number.

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136409-47-7Relevant academic research and scientific papers

Novel synthesis of C-Nucleosides via radical coupling reaction

Togo, Hideo,Fujii, Misa,Ikuma, Toshihiro,Yokoyama, Masataka

, p. 3377 - 3380 (1991)

Photolysis of O-acyl-N-hydroxy-2-thiopyridone, derived from 2-tetrahydrofuryl carboxylic acid or 2,5 -anhydro -D -allonic acid, gave the corresponding C-nucleoside derivatives in the presence of heteroaromatic compounds via radical pathways.

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