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Glycine, N-(triphenylmethyl)-, triphenylmethyl ester, also known as N-triphenylmethylglycine triphenylmethyl ester, is a complex organic compound with the chemical formula C42H33NO2. It is a derivative of glycine, an amino acid, where the amino group is substituted with a triphenylmethyl group, and the carboxylic acid group is esterified with another triphenylmethyl group. Glycine, N-(triphenylmethyl)-, triphenylmethyl ester is characterized by its large, bulky triphenylmethyl groups, which can influence its physical and chemical properties, such as solubility and reactivity. It is typically synthesized for use in organic chemistry research, particularly in the study of peptide synthesis and as a protecting group in the synthesis of complex organic molecules. The compound's structure and properties make it a valuable tool in the development of new pharmaceuticals and other specialty chemicals.

3226-97-9

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3226-97-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3226-97-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,2 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3226-97:
(6*3)+(5*2)+(4*2)+(3*6)+(2*9)+(1*7)=79
79 % 10 = 9
So 3226-97-9 is a valid CAS Registry Number.

3226-97-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-tritylglycine trityl ester

1.2 Other means of identification

Product number -
Other names Trityl-glycin-tritylester

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:3226-97-9 SDS

3226-97-9Relevant academic research and scientific papers

TRITYLATION REACTIONS BASED ON METALLIC CATALYSIS

-

Page/Page column 21, (2010/11/25)

The invention relates to a method for preparing tritylated compounds in which protic functional groups are protected with the triphenylmethyl group, method based on the homogeneous catalysis exercised by salts or metal complexes in organic solvents. The invention relates in particular to a method for the selective tritylation of some groups, obtained both directly and by selective detritylation, with methods based on metallic catalysis. The application to amino acids, typical substrates not suitable to be subjected as such to homogeneous tritylations in organic solvents, indicates the ability of the method to extend also to hydrophilic substrates. The method allows to obtain with high yield pertrityl amino acids, N-tritylamino acids or amino acids tritylated only in lateral chain, compounds which heretofore were either difficult to obtain in aqueous solvents or obtainable through indirect methods. All, in any case, are important intermediates in peptide synthesis.

Efficient Synthesis of N-Triphenylmethyl α-Amino Acids

Mutter, Manfred,Hersperger, Rene

, p. 198 - 200 (2007/10/02)

A new one-pot synthesis of N-triphenylmethyl(trityl) α-amino acids 3 via their trityl ester 2 has been developed.

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