Cas 146566-61-2,β-alanine, N-<α-methyl-N-<<(2-methylcyclohexyl)oxy>carbonyl>-L-tryptophyl>-D-3-(phenylmethyl)-, phenylmethyl ester, (1S-trans)

146566-61-2

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Basic information

Product Name: β-alanine, N-<α-methyl-N-<<(2-methylcyclohexyl)oxy>carbonyl>-L-tryptophyl>-D-3-(phenylmethyl)-, phenylmethyl ester, (1S-trans)
Synonyms: β-alanine, N-<α-methyl-N-<<(2-methylcyclohexyl)oxy>carbonyl>-L-tryptophyl>-D-3-(phenylmethyl)-, phenylmethyl ester, (1S-trans)
CAS NO:146566-61-2
Molecular Formula:
Molecular Weight: 609.766
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: β-alanine, N-<α-methyl-N-<<(2-methylcyclohexyl)oxy>carbonyl>-L-tryptophyl>-D-3-(phenylmethyl)-, phenylmethyl ester, (1S-trans)(CAS DataBase Reference)
NIST Chemistry Reference: β-alanine, N-<α-methyl-N-<<(2-methylcyclohexyl)oxy>carbonyl>-L-tryptophyl>-D-3-(phenylmethyl)-, phenylmethyl ester, (1S-trans)(146566-61-2)
EPA Substance Registry System: β-alanine, N-<α-methyl-N-<<(2-methylcyclohexyl)oxy>carbonyl>-L-tryptophyl>-D-3-(phenylmethyl)-, phenylmethyl ester, (1S-trans)(146566-61-2)

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: 146566-61-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 146566-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,5,6 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 146566-61:
(8*1)+(7*4)+(6*6)+(5*5)+(4*6)+(3*6)+(2*6)+(1*1)=152
152 % 10 = 2
So 146566-61-2 is a valid CAS Registry Number.

146566-61-2Upstream product

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146566-61-2Relevant academic research and scientific papers

Cholecystokinin dipeptoid antagonists: Design, synthesis, and anxiolytic profile of some novel CCK-A and CCK-B selective and 'mixed' CCK-A/CCK-B antagonists

Boden,Higginbottom,Hill,Horwell,Hughes,Rees,Roberts,Singh,Suman-Chauhan,Woodruff

, p. 552 - 565 (2007/10/02)

The design, synthesis, and structure-activity relationships (SAR) for the development of selective dipeptoid ligands for both of the cholecystokinin (CCK) receptor subtypes CCK-A and CCK-B are described. The SAR developed is used to design a ligand with e

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