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121910-87-0

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121910-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121910-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,9,1 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 121910-87:
(8*1)+(7*2)+(6*1)+(5*9)+(4*1)+(3*0)+(2*8)+(1*7)=100
100 % 10 = 0
So 121910-87-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H5BrO2/c9-8-5-10-6-3-1-2-4-7(6)11-8/h1-5H

121910-87-0SDS

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 3-bromo-1,4-benzodioxine

1.2 Other means of identification

Product number -
Other names 2-Bromobenzo-1,4-dioxin

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:121910-87-0 SDS

121910-87-0Relevant articles and documents

A versatile catalyst system for enantioselective synthesis of 2-substituted 1,4-benzodioxanes

Chong, Eugene,Qu, Bo,Zhang, Yongda,Cannone, Zachary P.,Leung, Joyce C.,Tcyrulnikov, Sergei,Nguyen, Khoa D.,Haddad, Nizar,Biswas, Soumik,Hou, Xiaowen,Kaczanowska, Katarzyna,Chwalba, Micha?,Tracz, Andrzej,Czarnocki, Stefan,Song, Jinhua J.,Kozlowski, Marisa C.,Senanayake, Chris H.

, p. 4339 - 4345 (2019)

We report the synthesis of enantiomerically enriched 1,4-benzodioxanes containing alkyl, aryl, heteroaryl, and/or carbonyl substituents at the 2-position. The starting 1,4-benzodioxines were readily synthesized via ring closing metathesis using an efficient nitro-Grela catalyst at ppm levels. Excellent enantioselectivities of up to 99:1 er were obtained by using the versatile catalyst system [Ir(cod)Cl]2/BIDIME-dimer in the asymmetric hydrogenation of 2-substituted 1,4-benzodioxines. Furthermore, DFT calculations reveal that the selectivity of the process is controlled by the protonation step; and coordinating groups on the substrate may alter the interaction with the catalyst, resulting in a change in the facial selectivity.

Thio-substituted tricyclic and bicyclic aromatic methanesulfinyl derivatives

-

Page/Page column 31-32, (2008/06/13)

The present invention is related to chemical compositions, processes for the preparation thereof and uses of the composition. Particularly, the present invention relates to compositions of compounds of Formula (A): wherein Ar, Y, R1 and q are as defined herein; and their use in the treatment of diseases, including treatment of sleepiness, promotion of wakefulness, treatment of Parkinson's disease, cerebral ischemia, stroke, sleep apneas, eating disorders, stimulation of appetite and weight gain, treatment of attention deficit hyperactivity disorder ("ADHD"), enhancing function in disorders associated with hypofunctionality of the cerebral cortex, including, but not limited to, depression, schizophrenia, fatigue, in particular, fatigue associated with neurologic disease, such as multiple sclerosis, chronic fatigue syndrome, and improvement of cognitive dysfunction.

NIS or NBS mediated formation of halo acetals. A convenient method for the one pot disubstitution of 1,4-benzodioxin

Sergi Capilla,Hernandez, Nathalie,Pujol, Ma. Dolors

, p. 135 - 141 (2007/10/03)

2,3-Substituted-1,4-benzodioxins are easily obtained under mild conditions in one-pot reaction from 1,4-benzodioxin with electrophilic halogen as iodine (NIS) or bromine (NBS) and the appropriate alcohol or phenol, in dichloromethane.

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