Cas 132102-97-7,Ethyl (1R*,2S*,3S*)-2-Hydroxy-3-<(1-hydroxy-2-methylcyclohex-1-yl)methyl>-1,2-dimethylcyclopentanecarboxylate

132102-97-7

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Basic information

Product Name: Ethyl (1R^*,2S^*,3S^*)-2-Hydroxy-3-<(1-hydroxy-2-methylcyclohex-1-yl)methyl>-1,2-dimethylcyclopentanecarboxylate
Synonyms: Ethyl (1R^*,2S^*,3S^*)-2-Hydroxy-3-<(1-hydroxy-2-methylcyclohex-1-yl)methyl>-1,2-dimethylcyclopentanecarboxylate
CAS NO:132102-97-7
Molecular Formula:
Molecular Weight: 312.45
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: Ethyl (1R^*,2S^*,3S^*)-2-Hydroxy-3-<(1-hydroxy-2-methylcyclohex-1-yl)methyl>-1,2-dimethylcyclopentanecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: Ethyl (1R^*,2S^*,3S^*)-2-Hydroxy-3-<(1-hydroxy-2-methylcyclohex-1-yl)methyl>-1,2-dimethylcyclopentanecarboxylate(132102-97-7)
EPA Substance Registry System: Ethyl (1R^*,2S^*,3S^*)-2-Hydroxy-3-<(1-hydroxy-2-methylcyclohex-1-yl)methyl>-1,2-dimethylcyclopentanecarboxylate(132102-97-7)

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: 132102-97-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132102-97-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,1,0 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132102-97:
(8*1)+(7*3)+(6*2)+(5*1)+(4*0)+(3*2)+(2*9)+(1*7)=77
77 % 10 = 7
So 132102-97-7 is a valid CAS Registry Number.

132102-97-7Upstream product

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132102-97-7Relevant academic research and scientific papers

Sequential Radical Cyclization/Intermolecular Carbonyl Addition Reactions Initiated by Samarium(II) Iodide

Molander, Gary A.,Kenny, Caryn

, p. 1439 - 1445 (2007/10/02)

A sequential reductive coupling process promoted by samarium(II) iodide (SmI2) is described.Thus, ethyl 2-acetyl-2-methyl-5-hexenoate, upon treatment with SmI2 in the presence of a variety of aldehydes or ketones, undergoes an initial radical (ketyl) olef

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