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Carbamic acid, [(1S)-2-oxo-1-[[1-(phenylmethyl)-1H-imidazol-4-yl]methyl]-2-[[2-[(triphen ylmethyl)thio]ethyl]amino]ethyl]-, 9H-fluoren-9-ylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

827348-54-9

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827348-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 827348-54-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,7,3,4 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 827348-54:
(8*8)+(7*2)+(6*7)+(5*3)+(4*4)+(3*8)+(2*5)+(1*4)=189
189 % 10 = 9
So 827348-54-9 is a valid CAS Registry Number.

827348-54-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [(S)-2-(1-Benzyl-1H-imidazol-4-yl)-1-(2-tritylsulfanyl-ethylcarbamoyl)-ethyl]-carbamic acid 9H-fluoren-9-ylmethyl ester

1.2 Other means of identification

Product number -
Other names -

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:827348-54-9 SDS

827348-54-9Downstream Products

827348-54-9Relevant academic research and scientific papers

Modular synthesis of pantetheine and phosphopantetheine

Mandel, Alexander L.,La Clair, James J.,Burkart, Michael D.

, p. 4801 - 4803 (2007/10/03)

(Chemical Equation Presented) D-Pantetheine and D-phosphopantetheine, precursors to coenzyme A, have been synthesized though a linear sequence from three modules (M1-M3) in 9 and 10 steps, respectively. These routes provide access to analogues of coenzyme A containing modified cystamines, β-alanines, and pantoic acid residues. All three modules were joined using conventional methods of peptide synthesis. The chiral component, M3, was derived from D-pantolactone.

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