42729-96-4

Basic information

• Product Name: 3-ALLYL-2-HYDROXY-BENZOIC ACID
• Synonyms: 3-ALLYL-2-HYDROXY-BENZOIC ACID;RARECHEM AL BE 0937;2-Hydroxy-3-(prop-2-en-1-yl)benzoic acid
• CAS NO: 42729-96-4
• Molecular Formula: C₁₀H₁₀O₃
• Molecular Weight: 178.18
• Product Categories: pharmacetical
• Mol File: 42729-96-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 319.4°Cat760mmHg
• Flash Point: 161.2°C
• Appearance: /
• Density: 1.23g/cm³
• Vapor Pressure: 0.000141mmHg at 25°C
• Refractive Index: 1.591
• CAS DataBase Reference: 3-ALLYL-2-HYDROXY-BENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ALLYL-2-HYDROXY-BENZOIC ACID(42729-96-4)
• EPA Substance Registry System: 3-ALLYL-2-HYDROXY-BENZOIC ACID(42729-96-4)

Safety Data

• Hazardous Substances Data: 42729-96-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H10O3/c1-2-4-7-5-3-6-8(9(7)11)10(12)13/h2-3,5-6,11H,1,4H2,(H,12,13)

Upstream product

• 59086-52-1 2-allyloxybenzoic acid 
• 96400-13-4 ethyl 3-allyl-2-hydroxybenzoate 
• 31456-98-1 methyl 3-allyl-salicylate 
• 124-38-9 carbon dioxide 
• 413599-93-6 1-allyl-3-bromo-2-methoxymethoxybenzene 
• 119-36-8 methyl salicylate 
• 142273-81-2 1,3-dibromo-2-(methoxymethoxy)benzene 
• 608-33-3 2,6-dibromophenol 

Downstream Products

• 92810-83-8 2-hydroxy-3-propenyl-benzoic acid 
• 22890-52-4 3-(1-propyl)-2-hydroxybenzoic acid 
• 31457-03-1 2-methyl-2,3-dihydrobenzo[b]furan-7-carboxylic acid 
• 31457-07-5 2-methyl-7-benzofurancarbonsaeure 
• 82940-64-5 (E)-2-allyl-4-(phenyldiazenyl)phenol 
• 3383-04-8 1,3-di(prop-2-en-1-yl)-2-[(prop-2-en-1-yl)-oxy]benzene 
• 20490-22-6 2,4,6-tris(2-propenyl)phenol 
• 74663-50-6 2,4,6-tri-n-Propylphenol 
• 6626-32-0 2,6-di-n-propylphenol 
• 33567-59-8 (2-methoxy-phenyl)-acetaldehyde 
• 6380-21-8 2-(prop-1-enyl)phenol 
• 3383-05-9 allyl 2-allylphenyl ether 
• 3382-99-8 2,6-diallylphenol 
• 10577-44-3 2-(1-propenyl)anisole 

Relevant articles and documents

Small-molecules that covalently react with a human prolyl hydroxylase-towards activity modulation and substrate capture

We describe covalently binding modulators of the activity of human prolyl hydroxylase domain 2 (PHD2) and studies towards a strategy for photocapture of PHD2 substrates. Reversible active site binding of electrophile bearing compounds enables susbsequent covalent reaction with a lysine residue (K408) in the flexible C-terminal region of PHD2 to give a modified protein that retains catalytic activity.

Microwave-assisted rapid Claisen rearrarangement on solid phase

O-Allylsalicylic acids anchored to merrifield resin, are rapidly rearranged to the corresponding ortho-allylsalicylic acids in high yields for the first time under microwave irradiation.