Cas 140676-93-3,tricyclo<3.3.1.1<sup>3,7</sup>>dec-1-yl <R-(RS,SR)>-<2-<<1-(hydroxymethyl)-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>carbamate

140676-93-3

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Basic information

Product Name: tricyclo<3.3.1.1^3,7>dec-1-yl -<2-<<1-(hydroxymethyl)-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>carbamate
Synonyms:
CAS NO:140676-93-3
Molecular Formula:
Molecular Weight: 529.679
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: tricyclo<3.3.1.1^3,7>dec-1-yl -<2-<<1-(hydroxymethyl)-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>carbamate(CAS DataBase Reference)
NIST Chemistry Reference: tricyclo<3.3.1.1^3,7>dec-1-yl -<2-<<1-(hydroxymethyl)-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>carbamate(140676-93-3)
EPA Substance Registry System: tricyclo<3.3.1.1^3,7>dec-1-yl -<2-<<1-(hydroxymethyl)-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>carbamate(140676-93-3)

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: 140676-93-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 140676-93-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,7 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 140676-93:
(8*1)+(7*4)+(6*0)+(5*6)+(4*7)+(3*6)+(2*9)+(1*3)=133
133 % 10 = 3
So 140676-93-3 is a valid CAS Registry Number.

140676-93-3Upstream product

5854-52-4 1-adamantyl chloroformate

140676-93-3Downstream Products

140676-93-3Relevant 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 (1993)

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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