625095-57-0

Basic information

• Product Name: (S)-1-(3-Chlorophenyl)-1,3-propanediol
• Synonyms: (S)-1-(3-Chlorophenyl)-1,3-propanediol;(S)-1-(3-chlorophenyl)propane-1,3-diol
• CAS NO: 625095-57-0
• Molecular Formula: C₉H₁₁ClO₂
• Molecular Weight: 186.63544
• Mol File: 625095-57-0.mol
• Article Data: 11

Chemical Properties

• Melting Point: 142-144 °C
• Boiling Point: 345.3±27.0 °C(Predicted)
• Appearance: /
• Density: 1.274±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Store in freezer, under -20°C
• PKA: 13.68±0.20(Predicted)
• CAS DataBase Reference: (S)-1-(3-Chlorophenyl)-1,3-propanediol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-(3-Chlorophenyl)-1,3-propanediol(625095-57-0)
• EPA Substance Registry System: (S)-1-(3-Chlorophenyl)-1,3-propanediol(625095-57-0)

Safety Data

• Hazardous Substances Data: 625095-57-0(Hazardous Substances Data)

Usage

General Description

(S)-1-(3-Chlorophenyl)-1,3-propanediol, also known as triclosan, is a synthetic antibacterial and antifungal agent commonly used in personal care products such as soaps, toothpaste, and hand sanitizers. It is also utilized in certain industrial and medical applications. Triclosan works by inhibiting the growth of bacteria and fungi, making it an effective ingredient for products designed to kill or prevent the spread of harmful microorganisms. However, there is ongoing debate and research regarding the potential health and environmental concerns associated with triclosan, including its possible contribution to antibiotic resistance and disruption of hormone regulation in humans and wildlife. As a result, some jurisdictions have implemented regulations or bans on its use in certain products.

Upstream product

• 625095-56-9 (S)-(-)-(3-chlorophenyl)-3-hydroxypropionic acid 
• 804561-30-6 (2S,8R,11S)-2-(3-chlorophenyl)-8-methyl-11-(1-methylethyl)-1,5-dioxaspiro[5.5]undecane 
• 51699-45-7 (S)-(-)-1-(3'-Chlorophenyl)-1,3-Propanediol 
• 618-46-2 m-Chlorobenzoyl chloride 
• 33167-21-4 3-(3-chloro-phenyl)-3-oxo-propionic acid ethyl ester 
• 51699-40-2 3-(3-chlorophenyl)-3-hydroxypropionic acid ethyl ester 
• 13422-80-5 3-(3-chlorophenyl)-3-oxopropanoic acid 
• 587-04-2 m-Chlorobenzaldehyde 
• 99-02-5 3'-Chloroacetophenone 
• 804560-96-1 (+/-)-1-(1,3-bistrimethylsilyloxypropyl)-3-chlorobenzene 
• 108-05-4 vinyl acetate 
• 135505-20-3 (S)-(-)-methyl 3-(3-chlorophenyl)-3-hydroxypropanoate 
• 632327-19-6 methyl 3-(3-chlorophenyl)-3-oxopropanoate 
• 40620-64-2 3-hydroxy-3-(3'-chlorophenyl)propionic acid 

Downstream Products

• 693223-08-4 (4S)-(-)-trans-2-(4-nitrophenoxy)-2-oxo-4-(3-chlorophenyl)-1,3,2-dioxaphosphorinane 
• 883989-27-3 (±)-4-(3-chlorophenyl)-2-(4-nitrophenoxy)-1,3,2-dioxaphosphinane-2-oxide 
• 625095-60-5 (+)-cis-9-{2-[4-(S)-(3-chlorophenyl)-2-oxo-1,3,2-dioxaphosphorinan-2-methyleneoxy]eth-1-yl}adenine 
• 852948-13-1 [14C]-MB07811 
• 852948-12-0 (2S,4S)-2-[(3,5-dimethyl-4-(4'-hydroxy-3'-isopropylbenzyl)-phenoxy)methyl]-4-(3-chlorophenyl)-2-oxido[1,3,2]dioxaphosphane 
• 1233960-52-5 cis-3-O-[4-(S)-(3-chlorophenyl)-2-oxo-1,3,2-dioxaphosphorinan-2-yl]-18β-glycyrrhetinic acid 
• 1224724-30-4 5-biphenyl-4-yl-6-chloro-2-(4-(3-chlorophenyl)-2-oxo-2λ5-[1,3,2]-dioxaphosphinan-2-ylmethylsulfanyl)-1H-benzoimidazole 
• 1229578-27-1 C₂₂H₂₁ClNO₄PS 
• 1229578-26-0 C₂₂H₂₁ClNO₄PS 

Relevant articles and documents

PHENANTHROLINE PHOSPHONIC ACID DERIVATIVE AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF

The present invention relates to a novel phenanthroline phosphonic acid compound and a pharmaceutical salt thereof, as well as an application of the compound and the pharmaceutical salt thereof as collagen prolyl hydroxylase inhibitors in the preparation of drugs for preventing or treating collagen prolyl-4-hydroxylase related disease.

Design, Synthesis, and Sustained-Release Property of 1,3-Cyclic Propanyl Phosphate Ester of 18β-Glycyrrhetinic Acid

A new class of potential prodrugs, 1,3-cyclic propanyl phosphate esters of 18β-glycyrrhetic acid, was designed and synthesized through the key reaction of 18β-glycyrrhetic acid with 1,3-cyclic propanyl phosphate ester catalysed by lithium diisopropylamide

NOVEL 2'-C-METHYL AND 4'-C-METHYL NUCLEOSIDE DERIVATIVES

Novel 2'-C-methyl nucleoside 5 '-monophosphate and 4'-C-methyl nucleoside 5'- monophosphate derivatives, stereoisomers, and pharmaceutically acceptable salts or prodrugs thereof, their preparation, and their uses for the treatment of hepatitis C viral inf