Cas 126771-43-5,(S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-methyl-butyric acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester

126771-43-5

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Basic information

Product Name: (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-methyl-butyric acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester
Synonyms: (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-methyl-butyric acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester
CAS NO:126771-43-5
Molecular Formula:
Molecular Weight: 648.54
EINECS: N/A
Product Categories: N/A
Mol File: 126771-43-5.mol
Article Data: 1

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: (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-methyl-butyric acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-methyl-butyric acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester(126771-43-5)
EPA Substance Registry System: (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-methyl-butyric acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester(126771-43-5)

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: 126771-43-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 126771-43-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,7,7 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126771-43:
(8*1)+(7*2)+(6*6)+(5*7)+(4*7)+(3*1)+(2*4)+(1*3)=135
135 % 10 = 5
So 126771-43-5 is a valid CAS Registry Number.

126771-43-5Upstream product

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126771-43-5Relevant articles and documents

AN EFFICIENT METHOD FOR RACEMIZATION FREE ATTACHMENT OF 9-FLUORENYLMETHYLOXYCARBONYL-AMINO ACIDS TO PEPTIDE SYNTHESIS SUPPORTS

Bernatowicz, Michael S.,Kearney, Thomas,Neves, Richard S.,Koester, Hubert

, p. 4341 - 4344 (2007/10/02)

An efficient, general, and racemization free method of covalently attaching N α-Fmoc protected amino acids to solid supports for peptide synthesis is described.The process involves the preparation of 2,4-dichlorophenyl-N α-Fmoc- aminoacyl-4-oxymethyl-phen

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