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72912-33-5

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72912-33-5 Usage

General Description

1-[2-bromo-1-(1,1-dimethylethoxy)ethyl]-4-methoxybenzene is a chemical compound with the molecular formula C12H17BrO2. It is a white solid with a molecular weight of 281.16 g/mol. 1-[2-bromo-1-(1,1-dimethylethoxy)ethyl]-4-methoxybenzene is used in organic synthesis and pharmaceutical research as a building block for the synthesis of biologically active molecules. It contains a bromoethyl group and a methoxybenzene group, making it a versatile molecule for the modification of other organic compounds. The presence of the 1,1-dimethylethoxy group also makes it more stable and less prone to degradation, making it an ideal reagent for certain chemical reactions. Overall, this compound has potential applications in the pharmaceutical and chemical industries due to its reactivity and stability.

Check Digit Verification of cas no

The CAS Registry Mumber 72912-33-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,9,1 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 72912-33:
(7*7)+(6*2)+(5*9)+(4*1)+(3*2)+(2*3)+(1*3)=125
125 % 10 = 5
So 72912-33-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H19BrO2/c1-13(2,3)16-12(9-14)10-5-7-11(15-4)8-6-10/h5-8,12H,9H2,1-4H3

72912-33-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-bromo-1-[(2-methylpropan-2-yl)oxy]ethyl]-4-methoxybenzene

1.2 Other means of identification

Product number -
Other names EINECS 277-013-5

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:72912-33-5 SDS

72912-33-5Relevant articles and documents

Electrochemical Alkoxyhalogenation of Alkenes with Organohalides as the Halide Sources via Dehalogenation

Li, Jin-Heng,Li, Yang,Luo, Mu-Jia,Song, Ren-Jie,Zhang, Ting-Ting

supporting information, p. 7250 - 7254 (2020/10/05)

A general, ideal atom utilization electrochemical technology to enable alkene alkoxyhalogenation and organohalide dehalogenation in one pot is presented. This technology is highlighted by convergent strategy integrating several reactions, such as alkene alkoxyhalogenation, organohalide dehalogenation, and dehalogenation deuteration. Experimental data suggest that alkenes have the lowest oxidation potential, which lead to anodic conversion of the C═C bond to the radical cation intermediates, and cathodic transformations of organohalides, including alkyl and aryl halides, as the nucleophilic halogen sources.

Synthesis and renal vasodilator activity of some dopamine agonist 1-aryl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diols: Halogen and methyl analogues of fenoldopam

Weinstock,Ladd,Wilson,Brush,Yim,Gallagher Jr.,McCarthy,Silvestri,Sarau,Flaim

, p. 2315 - 2325 (2007/10/02)

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