Cas 1107613-57-9,(1R,2S)-tert-butyl 1-methyl-2-(2,4,6-trimethylbenzylamino) cyclopentanecarboxylate

1107613-57-9

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Basic information

Product Name: (1R,2S)-tert-butyl 1-methyl-2-(2,4,6-trimethylbenzylamino) cyclopentanecarboxylate
Synonyms: (1R,2S)-tert-butyl 1-methyl-2-(2,4,6-trimethylbenzylamino) cyclopentanecarboxylate
CAS NO:1107613-57-9
Molecular Formula:
Molecular Weight: 331.499
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: (1R,2S)-tert-butyl 1-methyl-2-(2,4,6-trimethylbenzylamino) cyclopentanecarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S)-tert-butyl 1-methyl-2-(2,4,6-trimethylbenzylamino) cyclopentanecarboxylate(1107613-57-9)
EPA Substance Registry System: (1R,2S)-tert-butyl 1-methyl-2-(2,4,6-trimethylbenzylamino) cyclopentanecarboxylate(1107613-57-9)

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: 1107613-57-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1107613-57-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,7,6,1 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1107613-57:
(9*1)+(8*1)+(7*0)+(6*7)+(5*6)+(4*1)+(3*3)+(2*5)+(1*7)=119
119 % 10 = 9
So 1107613-57-9 is a valid CAS Registry Number.

1107613-57-9Upstream product

1107613-57-9Downstream Products

1107613-57-9Relevant academic research and scientific papers

Asymmetric construction of quaternary carbon centers by sequential conjugate addition of lithium amide and in situ alkylation: Utility in the synthesis of (-)-aspidospermidine

Suzuki, Mayuko,Kawamoto, Yoshito,Sakai, Takeo,Yamamoto, Yasutomo,Tomioka, Kiyoshi

supporting information; experimental part, p. 653 - 655 (2009/08/08)

(Chemical Equation Presented) Chiral diether ligand-controlled asymmetric conjugate addition of a lithium amide to cyclopentenecarboxylate and subsequent in situ alkylation gave a chiral cyciopentane derivative bearing a quaternary carbon with high enanti

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