140128-20-7

Basic information

• Product Name: (Z)-2-(2-Boc-aminothiazole-4-yl-)-2-trityloxyiminoacetic acid
• Synonyms: (Z)-2-(2-BOC-AMINOTHIAZOLE-4-YL)-2-TRITYLOXYIMINO ACETIC ACID;BATT;BATT:(Z)-2-(2-BOC-AMINOTHIAZOLE-4-YL-)-2-TRITYLOXYIMINO ACETIC ACID;(Z)-2-[[(1,1-dimethylethoxy)carbonyl]amino]-alpha-[(triphenylmethoxy)imino]-4-thiazoleacetic acid
• CAS NO: 140128-20-7
• Molecular Formula: C₂₉H₂₇N₃O₅S
• Molecular Weight: 529.61
• Mol File: 140128-20-7.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Density: 1.24
• Refractive Index: 1.615
• CAS DataBase Reference: (Z)-2-(2-Boc-aminothiazole-4-yl-)-2-trityloxyiminoacetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-2-(2-Boc-aminothiazole-4-yl-)-2-trityloxyiminoacetic acid(140128-20-7)
• EPA Substance Registry System: (Z)-2-(2-Boc-aminothiazole-4-yl-)-2-trityloxyiminoacetic acid(140128-20-7)

Safety Data

• Hazardous Substances Data: 140128-20-7(Hazardous Substances Data)

Usage

General Description

The chemical compound "(Z)-2-(2-Boc-aminothiazole-4-yl-)-2-trityloxyiminoacetic acid" is an organic compound with a complex molecular structure. It contains a thiazole ring substituted with a Boc-protected amino group and a trityloxyiminoacetic acid moiety. The compound is also a Z-isomer, indicating the geometry of its double bonds. It is likely used in organic synthesis or medicinal chemistry as a building block or intermediate for the preparation of more complex molecules. Due to its specific structure and function, it may have potential applications in drug development or materials science.

InChI:InChI=1/C29H27N3O5S/c1-28(2,3)36-27(35)31-26-30-23(19-38-26)24(25(33)34)32-37-29(20-13-7-4-8-14-20,21-15-9-5-10-16-21)22-17-11-6-12-18-22/h4-19H,1-3H3,(H,33,34)(H,30,31,35)/b32-24-

Upstream product

• 76-83-5 trityl chloride 
• 140128-26-3 (2-tert-butoxycarbonylamino-thiazol-4-yl)-hydroxyimino-acetic acid 
• 186091-52-1 (2-tert-butoxycarbonylamino-thiazol-4-yl)-hydroxyimino-acetic acid ethyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 250597-69-4 (6R,7R)-3-Acetylsulfanyl-7-{2-(2-tert-butoxycarbonylamino-thiazol-4-yl)-2-[(Z)-trityloxyimino]-acetylamino}-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester 

Relevant articles and documents

Synthesis and antibacterial activities of novel C(3)-aminopyrimidinyl substituted cephalosporins including against respiratory tract pathogens

The variety of cephalosporins 1 and 2 which possessed C(3)-aminopyrimidinyl substituents were prepared and evaluated for their antibacterial activities. They exhibited excellent in vitro activities especially against respiratory tract pathogens such as penicillin resistant Streptococcus pneumonia, Moraxella catarrhalis and Haemophilus influenza. (C) 2000 Elsevier Science Ltd.