71269-07-3

Basic information

• Product Name: 3-(4-nitrophenyl)-2-propenyl chloride
• Synonyms: 3-(4-nitrophenyl)-2-propenyl chloride
• CAS NO: 71269-07-3
• Molecular Weight: 197.621
• Mol File: 71269-07-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-(4-nitrophenyl)-2-propenyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-nitrophenyl)-2-propenyl chloride(71269-07-3)
• EPA Substance Registry System: 3-(4-nitrophenyl)-2-propenyl chloride(71269-07-3)

Safety Data

• Hazardous Substances Data: 71269-07-3(Hazardous Substances Data)

Upstream product

• 35271-56-8 3-(4-nitrophenyl)propyl-2-en-1-ol 
• 882-06-4 4-nitro-trans-cinnamic acid 
• 35271-56-8 (E)-4-nitrocinnamyl alcohol 

Downstream Products

• 864528-41-6 (E)-1-(3-azidoprop-1-en-1-yl)-4-nitrobenzene 
• 35271-56-8 3-(4-nitrophenyl)propyl-2-en-1-ol 
• 123232-63-3 1-(4-nitrophenyl)-prop-2-en-1-ol 
• 194017-21-5 N-[3-(4-nitrophenyl)-2-propenyl]-N'-[bis(4-fluorophenyl)methyl]piperazine 
• 1446029-58-8 (E)-1-nitro-4-(4,4,4-trifluorobut-1-en-1-yl)benzene 
• 952682-84-7 C₂₀H₂₃N₃O₃ 

Relevant articles and documents

Ruthenium-catalyzed synthesis of allylic alcohols: Boronic acid as a hydroxide source

Secondary allylic alcohols were synthesized from linear allylic halides or carbonates using a catalytic amount of a ruthenium complex in the presence of boronic acid. The effects of solvent, base, ruthenium precursor, and boronic acid were fully explored, and the scope of the reaction was extended to various sub-strates. We also describe a preliminary investigation towards an enantioselective process.

CONFORMATIONALLY RESTRICTED AROMATIC INHIBITORS OF MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN AND METHOD

Novel compounds are provided which are inhibitors of MTP and thus are useful for lowering serum lipids and treating atherosclerosis and related diseases, and have the structure (I) or (IA) or (IB) including pharmaceutically acceptable salts thereof or prodrug esters thereof, wherein q is 0,1 or 2; R is H, alkyl, aryl or halogen; A is (1) a bond; (2) -O-; or (3) (i); B is: (ii) or (iii) or (iv) or (v) (wherein (a = 2, 3 or 4)) or (vi) or (vii) or (viii); and wherein L, L, R, R, R, R, R, R, R, R, R, X, (ix), (x) and (xi) are as defined herein.