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benzyl (-)-(2S)-1-trityl-aziridine-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67413-25-6

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67413-25-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67413-25-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,1 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67413-25:
(7*6)+(6*7)+(5*4)+(4*1)+(3*3)+(2*2)+(1*5)=126
126 % 10 = 6
So 67413-25-6 is a valid CAS Registry Number.

67413-25-6SDS

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 benzyl (-)-(2S)-1-trityl-aziridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names Benzyl (S)-N-tritylaziridine-2-carboxylate

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:67413-25-6 SDS

67413-25-6Relevant academic research and scientific papers

COVALENT RAS INHIBITORS AND USES THEREOF

-

Page/Page column 175, (2021/06/04)

The disclosure features compounds, or pharmaceutically acceptable salts thereof, alone and in combination with other therapeutic agents, pharmaceutical compositions, and protein conjugates thereof, capable of modulating biological processes including Ras, and their uses in the treatment of cancers.

RAS INHIBITORS

-

Paragraph 1530-1531, (2021/05/07)

The disclosure features macrocyclic compounds, and pharmaceutical compositions and protein complexes thereof, capable of inhibiting Ras proteins, and their uses in the treatment of cancers.

Genetic encoding of 2-aryl-5-carboxytetrazole-based protein photo-cross-linkers

Tian, Yulin,Lin, Qing

, p. 4449 - 4452 (2018/05/03)

Three γ-heteroatom-substituted N-methylpyrroletetrazole-lysines (mPyTXKs) were synthesized and subsequently incorporated into proteins site-specifically via genetic code expansion. The γ-seleno-substituted derivative, mPyTSeK, showed excellent incorporati

A convenient method of preparing optically active (S)-N-tritylaziridine- 2-carboxylate esters from (S)-β-haloamino acids

Kato, Yasuo,Fukumoto, Kenji

, p. 245 - 246 (2007/10/03)

A convenient method of preparing optically active (S)-N-tritylaziridine- 2-carboxylate esters via intramolecular cyclization of (S)-N-trityl-β- haloamino acid esters is described.

Synthesis of natural and non natural orthogonally protected lanthionines from N-tritylserine and allo-threonine derivatives

Dugave, Christophe,Menez, Andre

, p. 1453 - 1465 (2007/10/03)

The reactivity of electrophiles derived from N-tritylserine, threonine and allothreonine esters toward a selection of nucleophiles was investigated. Best yields from substitution products were obtained with N-trityliodoalanine and soft nucleophiles such a

One-step synthesis of optically active benzyl N-trityl-L-aziridine-2-carboxylic esters

Kuyl-Yeheskiely,Lodder,Van Der Marel,Van Boom

, p. 3013 - 3016 (2007/10/02)

Benzyl N-trityl-L-serine or threonine esters give upon treatment with sulphuryl chloride the corresponding benzyl (2s)-1-trityl-2-aziridine carboxylate or (2S, 3S)-1-trityl-3-methyl-2-aziridinecarboxylate esters in excellent yields.

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