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1363569-70-3

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1363569-70-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1363569-70-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,3,5,6 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1363569-70:
(9*1)+(8*3)+(7*6)+(6*3)+(5*5)+(4*6)+(3*9)+(2*7)+(1*0)=183
183 % 10 = 3
So 1363569-70-3 is a valid CAS Registry Number.

1363569-70-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromobenzyl 2'-bromobenzoate

1.2 Other means of identification

Product number -
Other names 2-bromobenzyl 2-bromobenzoate

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:1363569-70-3 SDS

1363569-70-3Downstream Products

1363569-70-3Relevant articles and documents

N-Heterocyclic Carbene Catalyzed Ester Synthesis from Organic Halides through Incorporation of Oxygen Atoms from Air

Tan, Hui,Wang, Shen-An,Yan, Zixi,Liu, Jianzhong,Wei, Jialiang,Song, Song,Jiao, Ning

supporting information, p. 2140 - 2144 (2020/12/01)

Oxygenation reactions with molecular oxygen (O2) as the oxygen source provides a green and straightforward strategy for the construction of O-containing compounds. Demonstrated here is a novel N-heterocyclic carbene (NHC) catalyzed oxidative transformation of simple and readily available organic halides into valuable esters through the incorporation of O-atoms from O2. Mechanistic studies prove that the deoxy Breslow intermediate generated in situ is oxidized to a Breslow intermediate for further transformation by this oxidative protocol. This method broadens the field of NHC catalysis and promotes oxygenation reactions with O2.

Pt, Pd and Au nanoparticles supported on a DNA-MMT hybrid: Efficient catalysts for highly selective oxidation of primary alcohols to aldehydes, acids and esters

Tang, Lin,Guo, Xuefeng,Li, Yunfeng,Zhang, Shuai,Zha, Zhenggen,Wang, Zhiyong

supporting information, p. 5213 - 5215 (2013/06/27)

Novel DNA-MMT hybrid supported metal nanoparticle catalysts, such as Pt/DNA-MMT, Pd/DNA-MMT, Au/DNA-MMT, were prepared for application in highly selective aerobic oxidation of primary alcohols to aldehydes, acids and esters, respectively. Taking advantage of the water-soluble reversibility of these catalysts, all the transformations could be performed smoothly in water and reuse of the catalysts has also been accomplished by a very simple phase separation process.

Dehydrogenation of alcohols under ambient atmosphere by a recyclable sol-gel encaged iridium pincer catalyst

Oded, Kobi,Musa, Sanaa,Gelman, Dmitri,Blum, Jochanan

experimental part, p. 68 - 70 (2012/06/16)

We demonstrate that a sol-gel entrapped iridium-pincer catalyst 1 is capable of promoting acceptorless dehydrogenation of primary and secondary alcohols. Although the dehydrogenations by the non-heterogenized catalyst are faster than by the sol-gel encaged complex, recyclability and significant stabilization of the organometallic species toward non-inert conditions represent a clear advantage from the environmental and practical points of view.

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