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129460-18-0

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129460-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129460-18-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,4,6 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 129460-18:
(8*1)+(7*2)+(6*9)+(5*4)+(4*6)+(3*0)+(2*1)+(1*8)=130
130 % 10 = 0
So 129460-18-0 is a valid CAS Registry Number.

129460-18-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Fmoc-Phe-OtBu

1.2 Other means of identification

Product number -
Other names Fmoc-Phe-Ot-Bu

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:129460-18-0 SDS

129460-18-0Downstream Products

129460-18-0Relevant articles and documents

Transition metal complexes as linkers for solid phase synthesis: Chromium carbonyl complexes as linkers for arenes

Comely,Gibson,Hales,Peplow

, p. 2526 - 2531 (2001)

Substrates containing aromatic rings have been attached to 'polymer supported triphenylphosphine' using a chromium carbonyl linker, chemically manipulated, and released from the polymer to demonstrate the potential use π-bound ligands in linker chemistry. Immobilisation of the phenylalanine derivative Fmoc-Phe-OtBu via its aromatic ring has been achieved and the resulting resin successfully subjected to standard amino acid deprotection and coupling procedures.

Versatile selective α-carboxylic acid esterification of N-protected amino acids and peptides by alcalase

Nuijens, Timo,Cusan, Claudia,Kruijtzer, John A. W.,Rijkers, Dirk T. S.,Liskamp, Rob M. J.,Quaedflieg, Peter J. L. M.

scheme or table, p. 809 - 814 (2009/07/11)

Under continuous removal of water, the industrial protease Alcalase allows selective synthesis of α-carboxylic acid methyl, ethyl, benzyl, allyl, 2-(trimethylsilyl)ethyl, and tert-butyl esters of amino acids and peptides under mild conditions in very high

A mild and selective method for the cleavage of tert-butyl esters

Jackson, Randy W

, p. 5163 - 5165 (2007/10/03)

A method for the cleavage of t-butyl esters using silica gel in refluxing toluene is reported. Good yields of the corresponding carboxylic acids are obtained, and the reaction is selective for t-butyl esters over t-butyl ethers and trimethylsilylethyl (TMSE) esters.

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