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16251-32-4

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16251-32-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16251-32-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,5 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16251-32:
(7*1)+(6*6)+(5*2)+(4*5)+(3*1)+(2*3)+(1*2)=84
84 % 10 = 4
So 16251-32-4 is a valid CAS Registry Number.

16251-32-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-phenoxyphenyl)propan-1-ol

1.2 Other means of identification

Product number -
Other names 3-(4-Phenoxy-phenyl)-propan-1-ol

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:16251-32-4 SDS

16251-32-4Relevant academic research and scientific papers

Preparation method of 3-aryl propanol

-

, (2017/08/28)

The invention discloses a preparation method of 3-aryl propanol. According to the preparation method, 3-aryl benzaldehyde and acetate are dissolved into an organic solvent, a catalyst is added at a certain temperature to carry out condensation reactions to prepare 3-aryl-2-alkene ester, then 3-aryl-2-alkene ester and a reducing agent carry out reduction reactions to obtain the final product 3-aryl propanol. The provided method adopts aryloxy to replace benzaldehyde to carry out condensation reactions with acetate, and then the reaction product is reduced to prepare 3-aryl propanol. Aromatic aldehyde and acetate carry out condensation reactions in the presence of a catalyst to prepare a Knoevenagel like condensate namely 3-aryl-2-alkene ester, and then 3-aryl-2-alkene ester is reduced by a reducing agent to prepare aryl propanol. The total yield is greater than 80%. The content is more than 95%. The raw materials are cheap, and the sources are wide. The preparation method is safer and more convenient. Moreover, the production cost is low, the raw materials is nontoxic or little toxic, the total yield is high, the generated waste gas, waste water, and waste solid are little, and the industrialization is easy.

PHARMACEUTICALLY ACTIVE COMPOUNDS AS DAG-LIPASE INHIBITORS

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Paragraph 0125, (2016/12/01)

The present invention relates to novel compounds which are highly selective inhibitors of diacylglycerol lipase α and β. These compounds are suitable for the treatment or prevention of disorders associated with, accompanied by or caused by increased 2-arachidonoylglycerol levels. Diacylglycerol lipase-α (alternative name: Sn1-specific diacylglycerol hydrolase a; DAGL-α) and -β are enzymes responsible for the biosynthesis of the endocannabinoid 2-arachidonoylglycerol. Selective and reversible inhibitors are required to study the function of DAGLs in neuronal cells in an acute and temporal fashion. The inventive ompounds are in particular suitable for the treatment of neurodegenerative diseases, inflammatory diseases, drug abuse and impaired energy balance, such as obesity.

Phosphonosulfonates are potent, selective inhibitors of dehydrosqualene synthase and staphyloxanthin biosynthesis in staphylococcus aureus

Song, Yongcheng,Lin, Fu-Yang,Yin, Fenglin,Hensler, Mary,Poveda, Carlos A. Rodrígues,Mukkamala, Dushyant,Cao, Rong,Wang, Hong,Morita, Craig T.,Pacanowska, Dolores González,Nizet, Victor,Oldfield, Eric

experimental part, p. 976 - 988 (2009/12/04)

Staphylococcus aureus produces a golden carotenoid virulence factor called staphyloxanthin (STX), and we report here the inhibition of the enzyme, dehydrosqualene synthase (CrtM), responsible for the first committed step in STX biosynthesis. The most acti

Design, synthesis and cytotoxicity of 7-deoxy aryl discodermolide analogues

Burlingame, Mark A.,Shaw, Simon J.,Sundermann, Kurt F.,Zhang, Dan,Petryka, Joseph,Mendoza, Esteban,Liu, Fenghua,Myles, David C.,LaMarche, Matthew J.,Hirose, Tomoyasu,Freeze, B. Scott,Smith III, Amos B.

, p. 2335 - 2338 (2007/10/03)

A series of 7-deoxy discodermolide analogues in which the lactone fragment 'C' was replaced by aryl substituents were designed, synthesized, and evaluated for cytotoxicity.

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