Cas 848137-12-2,[(2R,3R)-1-((2R,3R)-1-Isopropylcarbamoyl-2,3-diphenyl-cyclopropylcarbamoyl)-2,3-diphenyl-cyclopropyl]-carbamic acid tert-butyl ester

848137-12-2

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Basic information

Product Name: [(2R,3R)-1-((2R,3R)-1-Isopropylcarbamoyl-2,3-diphenyl-cyclopropylcarbamoyl)-2,3-diphenyl-cyclopropyl]-carbamic acid tert-butyl ester
Synonyms: [(2R,3R)-1-((2R,3R)-1-Isopropylcarbamoyl-2,3-diphenyl-cyclopropylcarbamoyl)-2,3-diphenyl-cyclopropyl]-carbamic acid tert-butyl ester
CAS NO:848137-12-2
Molecular Formula:
Molecular Weight: 629.799
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: [(2R,3R)-1-((2R,3R)-1-Isopropylcarbamoyl-2,3-diphenyl-cyclopropylcarbamoyl)-2,3-diphenyl-cyclopropyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(2R,3R)-1-((2R,3R)-1-Isopropylcarbamoyl-2,3-diphenyl-cyclopropylcarbamoyl)-2,3-diphenyl-cyclopropyl]-carbamic acid tert-butyl ester(848137-12-2)
EPA Substance Registry System: [(2R,3R)-1-((2R,3R)-1-Isopropylcarbamoyl-2,3-diphenyl-cyclopropylcarbamoyl)-2,3-diphenyl-cyclopropyl]-carbamic acid tert-butyl ester(848137-12-2)

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: 848137-12-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 848137-12-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,1,3 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 848137-12:
(8*8)+(7*4)+(6*8)+(5*1)+(4*3)+(3*7)+(2*1)+(1*2)=182
182 % 10 = 2
So 848137-12-2 is a valid CAS Registry Number.

848137-12-2Upstream product

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848137-12-2Relevant academic research and scientific papers

Turn and helical peptide handedness governed exclusively by side-chain chiral centers

Royo, Soledad,De Borggraeve, Wim M.,Peggion, Cristina,Formaggio, Fernando,Crisma, Marco,Jimenez, Ana I.,Cativiela, Carlos,Toniolo, Claudio

, p. 2036 - 2037 (2007/10/03)

We have examined the preferred 3D structure of homopeptides based on an α-amino acid lacking the asymmetry at the α-carbon but exhibiting chirality in the side chains (at the two β-carbons). These joint stereochemical properties are remarkably unusual for

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