Cas 144027-66-7,(2RS,3SR,6Ξ)-3-amino-2-(4-biphenylyl)-3,6-piperidine dicarboxylic acid dihydrochloride

144027-66-7

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Basic information

Product Name: (2RS,3SR,6Ξ)-3-amino-2-(4-biphenylyl)-3,6-piperidine dicarboxylic acid dihydrochloride
Synonyms:
CAS NO:144027-66-7
Molecular Formula:
Molecular Weight: 413.301
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: (2RS,3SR,6Ξ)-3-amino-2-(4-biphenylyl)-3,6-piperidine dicarboxylic acid dihydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: (2RS,3SR,6Ξ)-3-amino-2-(4-biphenylyl)-3,6-piperidine dicarboxylic acid dihydrochloride(144027-66-7)
EPA Substance Registry System: (2RS,3SR,6Ξ)-3-amino-2-(4-biphenylyl)-3,6-piperidine dicarboxylic acid dihydrochloride(144027-66-7)

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: 144027-66-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 144027-66-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,0,2 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 144027-66:
(8*1)+(7*4)+(6*4)+(5*0)+(4*2)+(3*7)+(2*6)+(1*6)=107
107 % 10 = 7
So 144027-66-7 is a valid CAS Registry Number.

144027-66-7Upstream product

144027-65-6 (2RS,3SR,6Ξ)-3-amino-2-(4-biphenylyl)-3,6-piperidine dicarboxylic acid dimethyl ester

144027-66-7Downstream Products

144027-66-7Relevant academic research and scientific papers

Preparation of novel heterocyclic amino acids from N-(arylmethylene) dehydroalanine methyl esters

Wulff, Guenter,Klinken, Heinz Theo

, p. 5985 - 5990 (2007/10/02)

N-(Arylmethylene)dehydroalanine methyl esters undergo a stereoregulated dimerization reaction to produce heterocyclic α,α′-diaminodicarboxylic acid derivatives. Further transformation yields stable hydrochlorides of free α,α′-diaminodicarboxyli acids whic

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