Cas 876404-32-9,2-<i>tert</i>-butoxycarbonylamino-3-[2-(3,3-diphenyl-propionyl)-1-(2-methoxy-ethoxymethyl)-1<i>H</i>-imidazol-4-yl]-3-hydroxy-propionic acid methyl ester

876404-32-9

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Basic information

Product Name: 2-tert-butoxycarbonylamino-3-[2-(3,3-diphenyl-propionyl)-1-(2-methoxy-ethoxymethyl)-1H-imidazol-4-yl]-3-hydroxy-propionic acid methyl ester
Synonyms: 2-tert-butoxycarbonylamino-3-[2-(3,3-diphenyl-propionyl)-1-(2-methoxy-ethoxymethyl)-1H-imidazol-4-yl]-3-hydroxy-propionic acid methyl ester
CAS NO:876404-32-9
Molecular Formula:
Molecular Weight: 581.666
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: 2-tert-butoxycarbonylamino-3-[2-(3,3-diphenyl-propionyl)-1-(2-methoxy-ethoxymethyl)-1H-imidazol-4-yl]-3-hydroxy-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-tert-butoxycarbonylamino-3-[2-(3,3-diphenyl-propionyl)-1-(2-methoxy-ethoxymethyl)-1H-imidazol-4-yl]-3-hydroxy-propionic acid methyl ester(876404-32-9)
EPA Substance Registry System: 2-tert-butoxycarbonylamino-3-[2-(3,3-diphenyl-propionyl)-1-(2-methoxy-ethoxymethyl)-1H-imidazol-4-yl]-3-hydroxy-propionic acid methyl ester(876404-32-9)

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: 876404-32-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 876404-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,4,0 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 876404-32:
(8*8)+(7*7)+(6*6)+(5*4)+(4*0)+(3*4)+(2*3)+(1*2)=189
189 % 10 = 9
So 876404-32-9 is a valid CAS Registry Number.

876404-32-9Upstream product

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876404-32-9Relevant academic research and scientific papers

Side-chain modified analogues of histaprodifen: Asymmetric synthesis and histamine H1-receptor activity

Patil, Rameshwar,Elz, Sigurd,Reiser, Oliver

, p. 672 - 676 (2007/10/03)

New analogues of histaprodifen with polar side chains have been stereoselectively synthesized and evaluated as histamine H1-receptor agonists. As a key transformation the asymmetric aminohydroxylation has been used, which was successfully reali

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