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(2S)-2-amino-4-(tritylsulfanyl)butanoic acid is a chiral organic compound with the molecular formula C22H23NO2S. It features a 2-amino-4-butanoic acid core, with a trityl (triphenylmethyl) group attached to the sulfur atom of a sulfanyl (thiol) group. (2S)-2-amino-4-(tritylsulfanyl)butanoic acid is significant in organic synthesis and medicinal chemistry due to its unique structure, which can be used as a building block for the synthesis of more complex molecules, particularly in the development of pharmaceuticals and other bioactive compounds. The trityl group provides a bulky, electron-rich substituent that can influence the reactivity and selectivity of the molecule, making it a valuable tool in the hands of chemists for various applications.

69955-57-3

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69955-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69955-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,5 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69955-57:
(7*6)+(6*9)+(5*9)+(4*5)+(3*5)+(2*5)+(1*7)=193
193 % 10 = 3
So 69955-57-3 is a valid CAS Registry Number.

69955-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name S-triphenylmethyl-L-homocysteine

1.2 Other means of identification

Product number -
Other names (S)-2-amino-4-tritylsulfanyl-butyric acid

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:69955-57-3 SDS

69955-57-3Relevant academic research and scientific papers

S-NITROSOMERCAPTO COMPOUNDS AND RELATED DERIVATIVES

-

Page/Page column 110, (2010/01/07)

The present invention is directed to mercapto-based and S- nitrosomercapto-based SNO compounds and their derivatives, and their use in treating a lack of normal breathing control, including the treatment of apnea and hypoventilation associated with sleep, obesity, certain medicines and other medical conditions.

The first asymmetric syntheses of L-homocysteine and L-homocystine

Adamczyk, Maciej,Fishpaugh, Jeffrey R.,Thiruvazhi, Mohan

, p. 4151 - 4156 (2007/10/03)

Asymmetric syntheses of L-homocysteine 1 and L-homocystine 2 are described. Alkylation of the carbanion derived from Schollkopf reagent 3 and ensuing hydrolyses gave S-triphenylmethyl-L-homocysteine 6. Removal of the triphenylmethyl group gave L-homocysteine 1 and subsequent oxidation provided L-homocystine 2.

Somatostatin receptor-binding peptides labeled with technetium-99m: Chemistry and initial biological studies

Pearson, Daniel A.,Lister-James, John,McBride, William J.,Wilson, David M.,Martel, Lawrence J.,Civitello, Edgar R.,Taylor, John E.,Moyer, Brian R.,Dean, Richard T.

, p. 1361 - 1371 (2007/10/03)

The synthesis of peptides which possess a high affinity for the somatostatin receptor and contain a chelator for the radionuclide technetium- 99m is described. The target compounds were designed such that they would form stable, oxotechnetium(V) chelate c

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