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1226-91-1

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1226-91-1 Usage

Common uses

Flavoring agent in the food industry
Fragrance ingredient in perfumes and cosmetics

Flavor profile

Buttery and creamy taste

Health concerns

Classified as a respiratory sensitizer
May cause allergic reactions in some individuals

Potential health effects

Linked to lung disease and respiratory problems
Particularly in workers exposed to high levels in occupational settings

Safety measures

Proper safety measures and regulations should be in place to minimize risks associated with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 1226-91-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,2 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1226-91:
(6*1)+(5*2)+(4*2)+(3*6)+(2*9)+(1*1)=61
61 % 10 = 1
So 1226-91-1 is a valid CAS Registry Number.

1226-91-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1,5-diphenylpentane-1,5-dione

1.2 Other means of identification

Product number -
Other names 1,5-diphenyl-3-methyl-1,5-pentanedione

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:1226-91-1 SDS

1226-91-1Relevant articles and documents

In situ formed acetals facilitated direct Michael addition of unactivated ketones

Koppolu, Srinivasa Rao,Balamurugan, Rengarajan

, p. 1186 - 1192 (2017/02/10)

TfOH-promoted synthesis of 1,5-diketones by the Michael reaction of unactivated ketones with chalcones has been described. Acetals formed under HC(OMe)3/TfOH conditions generate the required enol-equivalents for a smooth Michael reaction. A wide array of symmetrical and unsymmetrical 1,5-diketones has been synthesised.

A new Br?nsted acid derived from squaric acid and its application to Mukaiyama aldol and Michael reactions

Cheon, Cheol Hong,Yamamoto, Hisashi

scheme or table, p. 3555 - 3558 (2009/10/26)

Bis-N-trifluoromethanesulfonyl squaramide was prepared as a new bench-stable strong Br?nsted acid and applied to the Br?nsted acid-catalyzed Mukaiyama aldol and Michael reactions with silyl enol ethers. The resulting Mukaiyama aldol products of aldehydes

The first michael addition of metal ketone enolates to α,β- unsaturated esters under catalytic conditions: Tin enolate with a catalytic amount of tetrabutylammonium bromide

Yasuda, Makoto,Ohigashi, Noriyuki,Shibata, Ikuya,Baba, Akio

, p. 2180 - 2181 (2007/10/03)

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