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106116-42-1

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106116-42-1 Usage

General Description

1-(BROMOMETHYL)-3-METHOXY-5-METHYLBENZENE, also known as 1-(bromomethyl)-3-methoxy-5-methylbenzene, is a chemical compound with the molecular formula C9H11BrO. It consists of a benzene ring with a bromomethyl group at position 1, a methoxy group at position 3, and a methyl group at position 5. 1-(BROMOMETHYL)-3-METHOXY-5-METHYLBENZENE is commonly used as a building block in organic synthesis and pharmaceutical research. It may also have potential applications in the development of new drugs and materials due to its unique structure and properties. However, it is important to handle 1-(bromomethyl)-3-methoxy-5-methylbenzene with care as it is a potentially hazardous chemical and should only be used by trained professionals in a controlled laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 106116-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,1,1 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106116-42:
(8*1)+(7*0)+(6*6)+(5*1)+(4*1)+(3*6)+(2*4)+(1*2)=81
81 % 10 = 1
So 106116-42-1 is a valid CAS Registry Number.

106116-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Bromomethyl)-3-methoxy-5-methylbenzene

1.2 Other means of identification

Product number -
Other names 3-Methoxy-5-methylbenzylbromid

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:106116-42-1 SDS

106116-42-1Relevant articles and documents

Reactions of [2-(2-Naphthyl)phenyl]acetylenes and 2-(2-Naphthyl)benzaldehyde O-Phenyloximes: Synthesis of the Angucycline Tetrangulol and 1,10,12-Trimethoxy-8-methylbenzo[c]phenanthridine

Ngwira, Kennedy J.,Rousseau, Amanda L.,Johnson, Myron M.,de Koning, Charles B.

, p. 1479 - 1488 (2017)

The Suzuki–Miyaura coupling reaction between (1,4,5-trimethoxynaphthalen-2-yl)boronic acid and 2-iodo-3-methoxy-5-methylbenzaldehyde gave the intermediate 3-methoxy-5-methyl-2-(1,4,5-trimethoxynaphthalen-2-yl)benzaldehyde. Conversion of this benzaldehyde

Roles of the synergistic reductive O-methyltransferase GilM and of O-methyltransferase GilMT in the gilvocarcin biosynthetic pathway

Tibrewal, Nidhi,Downey, Theresa E.,Van Lanen, Steven G.,Ul Sharif, Ehesan,O'Doherty, George A.,Rohr, Juergen

supporting information; experimental part, p. 12402 - 12405 (2012/09/05)

Two enzymes of the gilvocarcin biosynthetic pathway, GilMT and GilM, with unclear functions were investigated by in vitro studies using purified, recombinant enzymes along with synthetically prepared intermediates. The studies revealed GilMT as a typical

NEW BRADYKININ B1 ANTAGONISTS

-

Page/Page column 162, (2010/04/03)

The invention relates to compounds of formula (I) where in R1, R1a, R1b, R2, R3 and X, X1, X2, X3 have the meaning as cited in the description and the claims. Said compounds are useful as Bradykinin B1 antagonists. The invention also relates to pharmaceutical compositions, the preparation of such compounds as well as the production and use as medicament.

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