Cas 26565-65-1,methyl 2-(1-cyclohexyl-2-oxo-2,4,5,6,7,7a-hexahydro-1H-indol-3-yl)acetate

26565-65-1

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Basic information

Product Name: methyl 2-(1-cyclohexyl-2-oxo-2,4,5,6,7,7a-hexahydro-1H-indol-3-yl)acetate
Synonyms: methyl 2-(1-cyclohexyl-2-oxo-2,4,5,6,7,7a-hexahydro-1H-indol-3-yl)acetate
CAS NO:26565-65-1
Molecular Formula:
Molecular Weight: 291.39
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 2-(1-cyclohexyl-2-oxo-2,4,5,6,7,7a-hexahydro-1H-indol-3-yl)acetate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-(1-cyclohexyl-2-oxo-2,4,5,6,7,7a-hexahydro-1H-indol-3-yl)acetate(26565-65-1)
EPA Substance Registry System: methyl 2-(1-cyclohexyl-2-oxo-2,4,5,6,7,7a-hexahydro-1H-indol-3-yl)acetate(26565-65-1)

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: 26565-65-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 26565-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,6 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26565-65:
(7*2)+(6*6)+(5*5)+(4*6)+(3*5)+(2*6)+(1*5)=131
131 % 10 = 1
So 26565-65-1 is a valid CAS Registry Number.

26565-65-1Upstream product

101-83-7 N-cyclohexyl-cyclohexanamine

26565-65-1Downstream Products

26565-65-1Relevant academic research and scientific papers

Direct Use of Unprotected Aliphatic Amines to Generate N-Heterocycles via β-C-H Malonylation with Iodonium Ylide

Zhao, Zhiguo,Kong, Xiangjin,Wang, Wei,Hao, Jingcheng,Wang, Yao

, p. 230 - 233 (2020)

An unprecedented method that enables the direct transformation of unprotected secondary aliphatic amines into functionalized N-heterocycles in the absence of transition metals was developed. The activation of these NH-free amines by the iodonium ylide ind

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