Cas 140850-82-4,carbamic acid, <2-<<1-(hydroxymethyl)-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>-, 2-methylcyclohexyl ester

140850-82-4

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Basic information

Product Name: carbamic acid, <2-<<1-(hydroxymethyl)-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>-, 2-methylcyclohexyl ester
Synonyms:
CAS NO:140850-82-4
Molecular Formula:
Molecular Weight: 491.63
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: carbamic acid, <2-<<1-(hydroxymethyl)-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>-, 2-methylcyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: carbamic acid, <2-<<1-(hydroxymethyl)-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>-, 2-methylcyclohexyl ester(140850-82-4)
EPA Substance Registry System: carbamic acid, <2-<<1-(hydroxymethyl)-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>-, 2-methylcyclohexyl ester(140850-82-4)

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: 140850-82-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 140850-82-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,8,5 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 140850-82:
(8*1)+(7*4)+(6*0)+(5*8)+(4*5)+(3*0)+(2*8)+(1*2)=114
114 % 10 = 4
So 140850-82-4 is a valid CAS Registry Number.

140850-82-4Upstream product

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140850-82-4Relevant 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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