Cas 115010-46-3,(S)-Thiophosphoric acid S-((1S,5R)-6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-ylmethyl) ester O-methyl ester O'-(4-nitro-phenyl) ester

115010-46-3

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Basic information

Product Name: (S)-Thiophosphoric acid S-((1S,5R)-6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-ylmethyl) ester O-methyl ester O'-(4-nitro-phenyl) ester
Synonyms:
CAS NO:115010-46-3
Molecular Formula:
Molecular Weight: 383.405
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: (S)-Thiophosphoric acid S-((1S,5R)-6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-ylmethyl) ester O-methyl ester O'-(4-nitro-phenyl) ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-Thiophosphoric acid S-((1S,5R)-6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-ylmethyl) ester O-methyl ester O'-(4-nitro-phenyl) ester(115010-46-3)
EPA Substance Registry System: (S)-Thiophosphoric acid S-((1S,5R)-6,6-dimethyl-bicyclo[3.1.1]hept-2-en-2-ylmethyl) ester O-methyl ester O'-(4-nitro-phenyl) ester(115010-46-3)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 115010-46-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 115010-46-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,0,1 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 115010-46:
(8*1)+(7*1)+(6*5)+(5*0)+(4*1)+(3*0)+(2*4)+(1*6)=63
63 % 10 = 3
So 115010-46-3 is a valid CAS Registry Number.

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115010-46-3Relevant academic research and scientific papers

A GENERAL CONFIGURATIONAL ANALYSIS OF O-SUBSTITUTED THIOPHOPHATES

Cullis, Paul M.,Misra, Rajinder,Wilkins, David J.

, p. 4211 - 4214 (1987)

O-Substituted thiophosphates can be configurationally analysed by 31P n.m.r. spectroscopy after S-alkylation with myrtenyl bromide followed by O-derivatisation either with dimethyl sulphate, diphenyl diazomethane or benzoyl chloride.

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