Welcome to LookChem.com Sign In|Join Free

CAS

  • or

75154-68-6

Post Buying Request

75154-68-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

75154-68-6 Usage

Description

METHYL (S)-(-)-1-TRITYL-2-AZIRIDINE-, also known as Methyl (S)-N-Tritylaziridine-2-carboxylate (CAS# 75154-68-6), is an off-white solid compound that is useful in organic synthesis. It is a chiral molecule with a trityl group attached to a methyl aziridine ring, which makes it a valuable building block for the creation of various complex organic molecules.

Uses

Used in Organic Synthesis:
METHYL (S)-(-)-1-TRITYL-2-AZIRIDINEis used as a synthetic building block for the development of complex organic molecules. Its unique structure and chirality make it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, METHYL (S)-(-)-1-TRITYL-2-AZIRIDINEis used as a key intermediate in the synthesis of various drugs. Its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial for the development of effective and safe medications.
Used in Agrochemical Industry:
METHYL (S)-(-)-1-TRITYL-2-AZIRIDINEis also utilized in the agrochemical industry for the synthesis of chiral pesticides and other agrochemical products. Its unique structure enables the development of more targeted and environmentally friendly solutions for pest control and crop protection.
Used in Research and Development:
In the research and development sector, METHYL (S)-(-)-1-TRITYL-2-AZIRIDINEserves as an important compound for studying the properties and reactivity of chiral molecules. Its use in various chemical reactions can provide valuable insights into the mechanisms of enantioselective synthesis and help develop new methods for the production of enantiomerically pure compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 75154-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,5 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75154-68:
(7*7)+(6*5)+(5*1)+(4*5)+(3*4)+(2*6)+(1*8)=136
136 % 10 = 6
So 75154-68-6 is a valid CAS Registry Number.
InChI:InChI=1/C23H21NO2/c1-26-22(25)21-17-24(21)23(18-11-5-2-6-12-18,19-13-7-3-8-14-19)20-15-9-4-10-16-20/h2-16,21H,17H2,1H3/t21-,24?/m0/s1

75154-68-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (516015)  Methyl(S)-(−)-1-tritylaziridine-2-carboxylate  98%

  • 75154-68-6

  • 516015-5G

  • 969.93CNY

  • Detail

75154-68-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl (S)-N-Tritylaziridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names methyl (2S)-1-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:75154-68-6 SDS

75154-68-6Relevant articles and documents

Synthesis and Stability of the Cyclic Sulfamidate of N-Trityl-L-Serine Methyl Ester

Pilkington, Melanie,Wallis, John D.

, p. 1857 - 1858 (1993)

The title compound 12, prepared in three steps from L-serine methyl ester, is thermally stable 50 deg C; the formation of the cyclic sulfamidite 9, rather than acyclic products, in the reaction of thionyl chloride with vic-amino alcohol 7 is far more de

Total synthesis and activity of the metallo-β-lactamase inhibitor aspergillomarasmine A

Koteva, Kalinka,King, Andrew M.,Capretta, Alfredo,Wright, Gerard D.

supporting information, p. 2210 - 2212 (2016/02/19)

Resistance to β-lactam antibiotics is mediated primarily by enzymes that hydrolytically inactivate the drugs by one of two mechanisms: serine nucleophilic attack or metal-dependent activation of a water molecule. Serine β-lactamases are countered in the c

KDM1A INHIBITORS FOR THE TREATMENT OF DISEASE

-

Paragraph 0571; 0572, (2016/09/26)

Disclosed herein are new compounds and compositions and their application as pharmaceuticals for the treatment of diseases. Methods of inhibition of KDM1A, methods of increasing gamma globin gene expression, and methods to induce differentiation of cancer cells in a human or animal subject are also provided for the treatment of diseases such as acute myelogenous leukemia.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 75154-68-6