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Cyclohexanone, 2,6-dibromo-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

41597-25-5

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41597-25-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41597-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,5,9 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 41597-25:
(7*4)+(6*1)+(5*5)+(4*9)+(3*7)+(2*2)+(1*5)=125
125 % 10 = 5
So 41597-25-5 is a valid CAS Registry Number.

41597-25-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dibromo-2-methylcyclohexan-1-one

1.2 Other means of identification

Product number -
Other names -

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:41597-25-5 SDS

41597-25-5Relevant academic research and scientific papers

TMS·OTf-Catalyzed α-bromination of carbonyl compounds by N-bromosuccinimide

Guha, Samar Kumar,Wu, Bo,Kim, Beom Soo,Baik, Woonphil,Koo, Sangho

, p. 291 - 293 (2007/10/03)

Various carbonyl compounds undergo α-bromination reaction under a mild and practical condition utilizing N-bromosuccinimide (NBS), catalyzed by trimethylsilyl trifluoromethanesulfonate (TMS·OTf). This method is also effective for the side-chain bromination of heteroaromatic carbonyl compounds without the ring brominations.

CONVENIENT PREPARATION OF 1,2-CYCLOHEXANEDIONES

Utaka, Masanori,Matsushita, Seishiro,Takeda, Akira

, p. 779 - 780 (2007/10/02)

1,2-Cyclohexanedione and 3-alkyl-1,2-cyclohexanediones were prepared in good to excellent yields from the corresponding 2,6-dibromocyclohexanones by treatment with aqueous NaOH.

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