Cas 141986-97-2,Methyl-phosphinic acid (1R,2S,3R,4R,5S,6R)-2,3,4,5,6-pentakis-benzyloxy-cyclohexyl ester

141986-97-2

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Basic information

Product Name: Methyl-phosphinic acid (1R,2S,3R,4R,5S,6R)-2,3,4,5,6-pentakis-benzyloxy-cyclohexyl ester
Synonyms: Methyl-phosphinic acid (1R,2S,3R,4R,5S,6R)-2,3,4,5,6-pentakis-benzyloxy-cyclohexyl ester
CAS NO:141986-97-2
Molecular Formula:
Molecular Weight: 692.789
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-phosphinic acid (1R,2S,3R,4R,5S,6R)-2,3,4,5,6-pentakis-benzyloxy-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Methyl-phosphinic acid (1R,2S,3R,4R,5S,6R)-2,3,4,5,6-pentakis-benzyloxy-cyclohexyl ester(141986-97-2)
EPA Substance Registry System: Methyl-phosphinic acid (1R,2S,3R,4R,5S,6R)-2,3,4,5,6-pentakis-benzyloxy-cyclohexyl ester(141986-97-2)

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: 141986-97-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141986-97-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,9,8 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 141986-97:
(8*1)+(7*4)+(6*1)+(5*9)+(4*8)+(3*6)+(2*9)+(1*7)=162
162 % 10 = 2
So 141986-97-2 is a valid CAS Registry Number.

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141986-97-2Relevant academic research and scientific papers

SYNTHESIS OF RACEMIC MYO-INOSITOL 1,4,5-TRISMETHYLPHOSPHONATE, MYO-INOSITOL 4,5-BISMETHYLPHOSPHONATE AND MYO-INOSITOL 5-METHYLPHOSPHONATE VIA A PHOSPHINATE APPROACH

Willems, Henrica A. M.,Veeneman, Gerrit H.,Westerduin, Pieter

, p. 2075 - 2078 (1992)

Synthesis of the (rac.) myo-inositol phosphate isosteric analogues 1,4,5-trismethyl phosphonate, 4,5-bismethylphosphonate, amd 5-methylphosphonate was accomplished using a phosphinate approach.

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