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134677-28-4

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134677-28-4 Usage

General Description

(S)-1-(3-Methoxyphenyl)propanol, also known as para-methoxyphenylpropanol or PMPP, is a chiral alcohol that is commonly used as a fragrance ingredient in perfumes and personal care products. It is a clear, colorless liquid with a floral, herbal odor. PMPP is known for its long-lasting scent and is often used as a fixative in fragrance formulations. It is also used in the synthesis of pharmaceuticals and agrochemicals. Additionally, PMPP is used as a flavoring agent in the food industry. The compound is considered safe for use in cosmetic products and is regulated by various authorities to ensure its safety for human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 134677-28-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,6,7 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 134677-28:
(8*1)+(7*3)+(6*4)+(5*6)+(4*7)+(3*7)+(2*2)+(1*8)=144
144 % 10 = 4
So 134677-28-4 is a valid CAS Registry Number.

134677-28-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-1-(3-methoxy-phenyl)-propan-1-ol

1.2 Other means of identification

Product number -
Other names .(S)-1-(3-methoxyphenyl)-1-propanol

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:134677-28-4 SDS

134677-28-4Downstream Products

134677-28-4Relevant articles and documents

Asymmetric amplification in catalysis by trans-1,2-diaminocyclohexane bistriflamide

Satyanarayana, Tummanapalli,Ferber, Benoit,Kagan, Henri B.

, p. 251 - 253 (2007)

(Figure Presented) A strong asymmetric amplification is observed in the addition of diethylzinc on aromatic aldehydes in the presence of the bistriflamide of trans-1,2-diaminocyclohexane 3a. The asymmetric amplification originates from the insolubility of

Solvent-free direct aza-Friedel-Crafts reactions between 3,4-dihydroisoquinoline and 1- or 2-naphthols

MacLeod, Patricia D.,Li, Zhiping,Feng, Jianqing,Li, Chao-Jun

, p. 6791 - 6794 (2006)

A self-catalytic aza-Friedel-Crafts method was employed to generate 1-naphtholyl tetrahydroisoquinoline products under neat conditions. In addition, a derivative was prepared in its enantiomerically pure form and has shown moderate activity for asymmetric catalysis in the asymmetric diethylzinc addition to aldehydes.

Deciphering the mechanism behind efficient enantioselective ethylation with thiazolidine-based amino alcohols

Cacho, Vanessa R. G.,Costa, Dora C. S.,Murtinho, Dina,Nunes, Sandra C. C.,Pais, Alberto A. C. C.,Silva Serra, M. Elisa,Tavares, Nélia C. T.

, (2022/01/08)

Taking advantage of the opposite chirality of two privileged starting materials, l-cysteine and d-penicillamine, a wide range of thiazolidine-based amino alcohols was synthesized. l-Cysteine derivatives were more efficient chiral inductors than the d-peni

Linear β-amino alcohol catalyst anchored on functionalized magnetite nanoparticles for enantioselective addition of dialkylzinc to aromatic aldehydes

Ciprioti, Stefano Vecchio,De Angelis, Martina,Di Pietro, Federica,Iannoni, Marika,Pilloni, Luciano,Primitivo, Ludovica,Ricelli, Alessandra,Righi, Francesco,Righi, Giuliana,Sappino, Carla,Suber, Lorenza

, p. 29688 - 29695 (2020/10/26)

A linear β-amino alcohol ligand, previously found to be a very efficient catalyst for enantioselective addition of dialkylzinc to aromatic aldehydes, has been anchored on differently functionalized superparamagnetic core-shell magnetite-silica nanoparticles (1a and 1b). Its catalytic activity in the addition of dialkylzinc to aldehydes has been evaluated, leading to promising results, especially in the case of 1b for which the recovery by simple magnetic decantation and reuse was successfully verified. This journal is

Enantioselective Addition of Diethylzinc to Aromatic Aldehydes Using Chiral Oxazoline-Based Ligands

Aydin, A. E.

, p. 1304 - 1312 (2020/10/02)

Abstract: Chiral oxazoline ligands containing an aromatic ring were prepared fromnorephedrine and pyrrole-2-carbonitrile or 2-hydroxybenzoyl chloride. Thesynthesized ligands were used in the copper-catalyzed asymmetric addition ofdiethylzinc to aromatic aldehydes to provide optically active 1-arylpropan-1-olswith high conversion (92%) and enantioselectivity (up to 99% ee).

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