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1-Pentanone, 3-ethyl-3-hydroxy-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91660-92-3

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91660-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91660-92-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,6 and 0 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 91660-92:
(7*9)+(6*1)+(5*6)+(4*6)+(3*0)+(2*9)+(1*2)=143
143 % 10 = 3
So 91660-92-3 is a valid CAS Registry Number.

91660-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-3-hydroxy-1-phenylpentan-1-one

1.2 Other means of identification

Product number -
Other names 3-ethyl-3-hydroxy-1-phenyl-1-pentanone

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:91660-92-3 SDS

91660-92-3Downstream Products

91660-92-3Relevant academic research and scientific papers

Strong counteranion effects on the catalytic activity of cationic silicon lewis acids in Mukaiyama aldol and Diels-Alder reactions

Hara, Kenji,Akiyama, Ryuto,Sawamura, Masaya

, p. 5621 - 5623 (2005)

(Graph Presented) A toluene-coordinated silyl borate, [Et 3Si(toluene)]B(C6F5)4, demonstrated catalytic activities significantly higher than those of Me3SiOTf and Me3SiNTf2 in Mu

ENOLBORONATES: NEW PRACTICAL REAGENTS FOR REGIOSELECTIVE ALDOL CONDENSATIONS.

Gennari, Cesare,Colombo, Lino,Poli, Giovanni

, p. 2279 - 2282 (2007/10/02)

Enolboronates, new enolates directly accessible from carbonyl compounds and giving aldol products regioselectively and in good yield with aliphatic and aromatic aldehydes, are described.

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