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L-Aspartic acid, N-[(1,1-dimethylethoxy)carbonyl]-, 1-(pentafluorophenyl) 4-(phenylmethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82825-48-7

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82825-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82825-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,2 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82825-48:
(7*8)+(6*2)+(5*8)+(4*2)+(3*5)+(2*4)+(1*8)=147
147 % 10 = 7
So 82825-48-7 is a valid CAS Registry Number.

82825-48-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Boc-L-Asp(Bzl)-OPfp

1.2 Other means of identification

Product number -
Other names Boc-Asp(OBzl)-OPfp

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:82825-48-7 SDS

82825-48-7Relevant academic research and scientific papers

Preparation of glycosyl amino acids as building blocks for the combinatorial synthesis of neoglycoconjugates

Ziegler, Thomas,Roeseling, Dirk,Subramanian, Lakshminarayanapuram R.

, p. 911 - 914 (2002)

Several neoglycosyl amino acids possessing a sugar residue, a spacer and a trifunctional amino acid moiety were synthesized both in solution and solid phase by activating the carboxylic group as its pentafluorophenyl ester for condensation. The methodolog

Multigram-scale synthesis of short peptides via a simplified repetitive solution-phase procedure

Meneses, Celia,Nicoll, Sarah L.,Trembleau, Laurent

supporting information; experimental part, p. 564 - 569 (2010/04/29)

(Chemical Equation Presented) A rapid repetitive solution-phase synthesis of peptides is described. The procedure involves coupling of amino acids and peptide acids, instead of the usual amino esters and peptide esters, to slight excesses of pentafluoroph

Aspartate Racemization in Synthetic Peptides. Part 2. Tendency to Racemization of Aminosuccinyl Residue

Schoen, Istvan,Szirtes, Tamas,Rill, Attila,Balogh, Gabor,Vadasz, Zsolt,et al.

, p. 3213 - 3223 (2007/10/02)

Aminosuccinyl (Asu) peptides, containing a strained ring system, are very vulnerable to epimerization and, during their formation, even as transients, in the presence of nucleophilic and nonnucleophilic bases, partial epimerization occurs.In the presence

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