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23546-36-3

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23546-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23546-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,4 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23546-36:
(7*2)+(6*3)+(5*5)+(4*4)+(3*6)+(2*3)+(1*6)=103
103 % 10 = 3
So 23546-36-3 is a valid CAS Registry Number.

23546-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,4-trimethyl-1-phenylpentan-3-one

1.2 Other means of identification

Product number -
Other names 1-phenyl-2,2,4-trimethyl-3-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:23546-36-3 SDS

23546-36-3Downstream Products

23546-36-3Relevant articles and documents

NON-CYCLIC HINDERED KETONES AS PERFUMING INGREDIENT

-

Page/Page column 9, (2010/02/14)

The present invention relates to the use as perfuming ingredient of a compound of formula (I) wherein R represents a hydrogen atom or a methyl or ethyl group, and R1 represents (i) a (Me)(R2)C=C(R3) group, R2 representing a hydrogen atom or a methyl group and R3 representing a methyl or ethyl group, or (ii) a phenyl group optionally substituted by one or two methyl groups; as well as to the compositions or articles associated with said compound.

Reductive cleavage of 2-methyleneoxetanes with lithium and 4,4'-di-tert- butylbiphenyl

Hashemzadeh, Mehrnoosh,Howell, Amy R.

, p. 1855 - 1858 (2007/10/03)

3,3-Dimethyl-2-mcthylene-4-phenyloxetane (5) undergoes reductive cleavage with lithium and 4,4'-di-tertbutylbiphenyl (DTBB) to give an intermediate dianion, which reacts regioselectively with aldehydes and ketones to give aldol adducts in modest yields. A

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