105960-29-0

Basic information

• Product Name: 3-Chloro-4-hydroxybenzyl alchol
• Synonyms: 3-Chloro-4-hydroxybenzyl alchol;BENZENEMETHANOL,3-CHLORO-4-HYDROXY;2-chloro-4-(hydroxymethyl)phenol
• CAS NO: 105960-29-0
• Molecular Formula: C₇H₇ClO₂
• Molecular Weight: 158.58228
• Mol File: 105960-29-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Chloro-4-hydroxybenzyl alchol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Chloro-4-hydroxybenzyl alchol(105960-29-0)
• EPA Substance Registry System: 3-Chloro-4-hydroxybenzyl alchol(105960-29-0)

Safety Data

• Hazardous Substances Data: 105960-29-0(Hazardous Substances Data)

Usage

General Description

3-Chloro-4-hydroxybenzyl alcohol, also known as Saligenin hydrochloride, is a chemical compound often used in organic synthesis. 3-Chloro-4-hydroxybenzyl alchol, which belongs to the class of organic compounds known as Phenylethanols, contains an aromatic ring with a hydroxyl group (-OH) and a benzyl alcohol group. The 3-Chloro-4-hydroxybenzyl alcohol is often identified by its CAS Registry Number, 1878-75-5. It is a relatively stable compound but should be stored in a cool, dry conditions in a well-sealed container to maintain its integrity. Its potential applications include use in the development of pharmaceuticals, agrochemicals, and dye intermediates among others. Common precautions should be taken when handling and storing this compound due to its reactivity potential.

Upstream product

• 50-00-0 formaldehyd 
• 95-57-8 2-monochlorophenol 
• 2420-16-8 4-hydroxy-3-chlorobenzaldehyde 
• 141805-79-0 3-Chlor-4-hydroxybenzylchlorid 
• 3964-57-6 methyl 4-hydroxy-3-chlorobenzoate 
• 99-76-3 methyl 4-hydroxylbenzoate 
• 3964-58-7 3-chloro-4-hydroxybenzoic acid 
• 59595-94-7 3?chloro?4-hydroxybenzoyl chloride 

Downstream Products

• 2787-77-1 4,4′-methylenebis(2-chlorophenol) 
• 2420-16-8 4-hydroxy-3-chlorobenzaldehyde 
• 148580-06-7 (2S,3S,4S,5R,6S)-3,4,5-Triacetoxy-6-(2-chloro-4-formyl-phenoxy)-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 148580-07-8 (2S,3S,4S,5R,6S)-3,4,5-Triacetoxy-6-(2-chloro-4-hydroxymethyl-phenoxy)-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 1054314-17-8 (2S,3S,4S,5R,6S)-3,4,5-Triacetoxy-6-[2-fluoro-4-(4-nitro-phenoxycarbonyloxymethyl)-phenoxy]-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 1053693-18-7 (2S,3S,4S,5R,6S)-3,4,5-Triacetoxy-6-[2-chloro-4-(2,5-dioxo-pyrrolidin-1-yloxycarbonyloxymethyl)-phenoxy]-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 1053634-04-0 C₄₂H₄₄FNO₂₀ 
• 1053697-83-8 C₄₈H₅₀FNO₂₃ 
• 213549-12-3 3-Chloro-4-[2-(4-nitrophenyl)ethoxycarbonyloxy]benzyl alcohol 
• 213547-97-8 3-Chloro-4-[2-(4-nitrophenyl)ethoxycarbonyloxy]benzyl vinyl ether 
• 213548-47-1 2'-O-[1-(3-chloro-4-hydroxybenzyloxy)ethyl]-3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)uridine 
• 213548-46-0 2'-O-(1-{3-chloro-4-[2-(4-nitrophenyl)ethoxycarbonyloxy]benzyloxy}ethyl)-3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)uridine 
• 3933-88-8 3,3',5,5'-Tetrachlor-4,4'-dihydroxydiphenylmethan 
• 91777-67-2 bis-(4-benzoyloxy-3-chloro-phenyl)-methane 

Relevant articles and documents

PRODRUGS OF FUSED-BICYCLIC C5aR ANTAGONISTS

The present disclosure provides, inter alia, Compounds of Formulae IA, IB, IC, IIA, IIB and IIC or pharmaceutically acceptable salts thereof that are modulators of the C5a receptor. Also provided are pharmaceutical compositions and methods of use including the treatment of diseases or disorders involving pathologic activation from C5a and non-pharmaceutical applications.

AROMATASE INHIBITOR

There is provided a compound of formula (I) wherein Z is selected from N and CR22, wherein R22 is H or a bond with D, wherein D is selected from a bond, C=O, and linear or branched hydrocarbon groups having a carbon chain of from 1 t

Acetals as New 2′-O-Protecting Functions for the Synthesis of Oligoribonucleotides: Synthesis of Uridine Building Blocks and Evaluation of Their Relative Acid Stability

A broad variety of new acyclic vinyl ethers (see 6-41) have been synthesized via the vinyl-interchange reaction of ethyl vinyl ether at room temperature using mercury(II) trifluoroacetate as a highly efficient catalyst. The appropriate vinyl ethers were r