Cas 81983-91-7,(S)-3-((1R,4R)-1-Chlorocarbonyl-4-methyl-3-oxo-cyclohexyl)-butyric acid methyl ester

81983-91-7

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Basic information

Product Name: (S)-3-((1R,4R)-1-Chlorocarbonyl-4-methyl-3-oxo-cyclohexyl)-butyric acid methyl ester
Synonyms:
CAS NO:81983-91-7
Molecular Formula:
Molecular Weight: 274.744
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)-3-((1R,4R)-1-Chlorocarbonyl-4-methyl-3-oxo-cyclohexyl)-butyric acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-((1R,4R)-1-Chlorocarbonyl-4-methyl-3-oxo-cyclohexyl)-butyric acid methyl ester(81983-91-7)
EPA Substance Registry System: (S)-3-((1R,4R)-1-Chlorocarbonyl-4-methyl-3-oxo-cyclohexyl)-butyric acid methyl ester(81983-91-7)

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: 81983-91-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 81983-91-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,9,8 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81983-91:
(7*8)+(6*1)+(5*9)+(4*8)+(3*3)+(2*9)+(1*1)=167
167 % 10 = 7
So 81983-91-7 is a valid CAS Registry Number.

81983-91-7Upstream product

81983-91-7Downstream Products

81983-86-0 3-((1S,4S)-1-Isobutyryl-4-methyl-3-oxo-cyclohexyl)-butyric acid methyl ester

81983-91-7Relevant academic research and scientific papers

Synthesis based on cyclohexadienes: Part 6 - A new total synthesis of (+/-)-methyl acorate and (+/-)-methyl epi-acorate

Ramanathan, Halasya,Rao, G S R Subba

, p. 901 - 905 (2007/10/02)

A new method of construction of carbon-carbon bond is described.Thus the dianions generated from the metal-ammonia reduction of substituted benzoic acids readily undergo Michael addition with methyl crotonate resulting in synthetically useful products hav

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