Cas 351006-60-5,1-benzoyl-1,4,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester

351006-60-5

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Basic information

Product Name: 1-benzoyl-1,4,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester
Synonyms: 1-benzoyl-1,4,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester
CAS NO:351006-60-5
Molecular Formula:
Molecular Weight: 259.305
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: 1-benzoyl-1,4,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-benzoyl-1,4,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester(351006-60-5)
EPA Substance Registry System: 1-benzoyl-1,4,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester(351006-60-5)

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: 351006-60-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 351006-60-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,0,0 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 351006-60:
(8*3)+(7*5)+(6*1)+(5*0)+(4*0)+(3*6)+(2*6)+(1*0)=95
95 % 10 = 5
So 351006-60-5 is a valid CAS Registry Number.

351006-60-5Upstream product

351006-60-5Downstream Products

116140-20-6 ethyl 1-benzoyl-3-piperidinecarboxylate

351006-60-5Relevant academic research and scientific papers

Asymmetric hydrogenation of pyridines: Enantioselective synthesis of nipecotic acid derivatives

Lei, Aiwen,Chen, Mao,He, Minsheng,Zhang, Xumu

, p. 4343 - 4347 (2007/10/03)

An asymmetric hydrogenation process of 3-substituted pyridine derivatives has been developed with the use of a Rh-TangPhos complex as the catalyst. The whole process consists of an efficient partial hydrogenation of nicotinate and a subsequent highly enan

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