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17131-52-1

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17131-52-1 Usage

General Description

3-(4-Methoxyphenoxy)-1,2-propanediol, also known as hexylresorcinol, is a chemical compound with the molecular formula C10H14O4. It is commonly used as a preservative in skincare and cosmetic products due to its antimicrobial and antioxidant properties. Hexylresorcinol is also utilized in pharmaceuticals as an antiseptic and local anesthetic, and as a food additive to prevent spoilage and microbial growth. Additionally, it has been studied for its potential role in the treatment of certain skin conditions and in cancer therapy. Overall, 3-(4-Methoxyphenoxy)-1,2-propanediol has a wide range of applications and is valued for its efficacy in inhibiting the growth of harmful microorganisms and potentially benefiting human health.

Check Digit Verification of cas no

The CAS Registry Mumber 17131-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,3 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17131-52:
(7*1)+(6*7)+(5*1)+(4*3)+(3*1)+(2*5)+(1*2)=81
81 % 10 = 1
So 17131-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O4/c1-13-9-2-4-10(5-3-9)14-7-8(12)6-11/h2-5,8,11-12H,6-7H2,1H3

17131-52-1 Well-known Company Product Price

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  • Aldrich

  • (210242)  3-(4-Methoxyphenoxy)-1,2-propanediol  ≥98%

  • 17131-52-1

  • 210242-10G

  • 1,037.79CNY

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17131-52-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Propanediol,3-(4-methoxyphenoxy)-

1.2 Other means of identification

Product number -
Other names 3-(4-methoxyphenoxy)-1,2-propanediol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:17131-52-1 SDS

17131-52-1Relevant articles and documents

Effective synthesis of non-racemic prenalterol based on spontaneous resolution of 3-(4-hydroxyphenoxy)propane-1,2-diol

Bredikhina, Zemfira A.,Kurenkov, Alexey V.,Bredikhin, Alexander A.

, p. 198 - 199 (2019/04/25)

Spontaneous resolution of rac-3-(4-hydroxyphenoxy)propane-1,2-diol has been successfully used in the synthesis of both enantiomers of chiral drug prenalterol.

Synthesis and some features of phase behavior of chiral p-alkoxyphenyl glycerol ethers

Fayzullin,Antonovich,Zakharychev,Bredikhina,Kurenkov,Bredikhin

, p. 202 - 209 (2015/04/14)

A series of (S)-3-(4-alkoxyphenoxy)propane-1,2-diols was prepared with the enantiomeric excess 86-92% by Sharpless asymmetric dihydroxylation of 1-alkoxy-4-allyloxybenzenes with an AD-mix-β mixture. R-Enantiomers with enantiomeric excess 97-99% and racemic samples were obtained by reaction of sodium p-substituted phenolates with (R)- and rac-3-chloropropane-1,2-diol. The phase behavior of racemates and scalemates in the produced homolog series of glycerol aryl ethers with hydrocarbon substituents of various length was examined by means of thermomicroscopy. The higher memberes of the homolog series of both racemic and scalemic diols undergo at heating an enantiotropic phase transition to a smectic liquid crystal phase.

Asymmetric hydrolytic kinetic resolution with recyclable polymeric Co(iii)-salen complexes: A practical strategy in the preparation of (S)-metoprolol, (S)-toliprolol and (S)-alprenolol: Computational rationale for enantioselectivity

Roy, Tamal,Barik, Sunirmal,Kumar, Manish,Kureshy, Rukhsana I.,Ganguly, Bishwajit,Khan, Noor-Ul H.,Abdi, Sayed H. R.,Bajaj, Hari C.

, p. 3899 - 3908 (2015/02/19)

A series of chiral polymeric Co(iii)-salen complexes based on a number of achiral and chiral linkers were synthesized and their catalytic performances were assessed in the asymmetric hydrolytic kinetic resolution of terminal epoxides. The effects of the linker were judiciously studied and it was found that in the case of the chiral BINOL-based polymeric salen complex 1, there was an enrichment in catalyst reactivity and enantioselectivity of the unreacted epoxide, particularly in the case of short as well as long chain aliphatic epoxides. Good isolated yields of the unreacted epoxide (up to 46% compared to 50% theoretical yield) along with high enantioselectivity (up to 99%) were obtained in most cases using catalyst 1. Further studies showed that catalyst 1 could retain its catalytic activity for six cycles under the present reaction conditions without any significant loss in activity or enantioselectivity. To show the practical applicability of the above synthesized catalyst we have synthesised some potent chiral β-blockers in moderate yield and high enantioselectivity using complex 1. The DFT (M06-L/6-31+G??//ONIOM(B3LYP/6-31G?:STO-3G)) calculations revealed that the chiral BINOL linker influences the enantioselectivity achieved with Co(iii)-salen complexes. Further, the transition state calculations show that the R-BINOL linker with the (S,S)-Co(iii)-salen complex is energetically preferred over the corresponding S-BINOL linker with the (S,S)-Co(iii)-salen complex for the HKR of 1,2-epoxyhexane. The role of non-covalent C-H?π interactions and steric effects has been discussed to control the HKR reaction of 1,2-epoxyhexane.

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