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90050-59-2

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90050-59-2 Usage

General Description

5-Bromo-2-methylbenzaldehyde is a chemical compound with the molecular formula C9H9BrO. It is a pale yellow solid that is commonly used as a building block in organic synthesis and as a reagent in chemical reactions. 5-Bromo-2-methylbenzaldehyde contains a benzene ring with a methyl group and a bromine atom attached to it, as well as an aldehyde functional group. Its structural properties make it useful in the production of pharmaceuticals, dyes, and other aromatic compounds. 5-Bromo-2-methylbenzaldehyde is also known for its characteristic odor and is used in fragrance and flavor applications. It is important to handle this chemical with care due to its potentially hazardous properties.

Check Digit Verification of cas no

The CAS Registry Mumber 90050-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,5 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90050-59:
(7*9)+(6*0)+(5*0)+(4*5)+(3*0)+(2*5)+(1*9)=102
102 % 10 = 2
So 90050-59-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7BrO/c1-6-2-3-8(9)4-7(6)5-10/h2-5H,1H3

90050-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-2-methylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 5-BROMO-2-METHYLBENZALDEHYDE

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:90050-59-2 SDS

90050-59-2Relevant articles and documents

SILANE COUPLING AGENT SYNTHESIS METHOD USING SELECTIVE SINGLE TERMINAL REACTION

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, (2020/04/24)

PROBLEM TO BE SOLVED: To provide an effective synthesis method of a silane coupling agent using a selective single terminal reaction to a both terminals equivalent compound without using expensive noble metal catalysts such as platinum and palladium in synthesis of novel silane coupling agent for adding high compatibility to a radical polymerizable monomer, and thereby adding high mechanical strength, flexibility (suppleness) and durability. SOLUTION: In a reaction for introducing a functional group only to a single terminal of a both terminals equivalent compound such as 1,10-decane diol for example, a nonuniform emulsion state is formed without adding an organic solvent for dissolving both substrates when reaction substrates are not dissolved each other and a reaction is processed at an emulsion boundary surface thereof. For generating the nonuniform emulsion state, the reaction is proceed at the emulsion boundary surface by using a microreactor element, a flow focusing device, a glass beads filling column or the like. SELECTED DRAWING: Figure 4 COPYRIGHT: (C)2020,JPOandINPIT

Catalyst system for producing polyethylene copolymers in a high temperature solution polymerization process

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Page/Page column 15; 16, (2019/06/10)

Catalyst system for producing ethylene copolymers in a high temperature solution process, the catalyst system comprising (i) a metallocene complex of formula (I) wherein M is Hf X is a sigma ligand, L is a bridge of the formula —SiR82—, wherein each R8 is independently a C1-C20-hydrocarbyl, tri(C1-C20-alkyl)silyl, C6-C20-aryl, C7-C20-arylalkyl or C7-C20-alkylaryl n is 0, 1 or 2 R1 and R1′ are the same or can be different and can be a linear or branched C1-C6-alkyl group, R2 and R2′ are the same or are different and are a CH2—R9 group, with R9 being H or linear or branched C1-C6-alkyl group R5 and R5′ are the same or are different and can be H or a linear or branched C1-C6-alkyl group or a OR group, wherein R is a C1-C6-alkyl group R6 and R6′ are the same or are different and can be H or a C(R10)3 group, with R10 being the same or different and R10 can be H or a linear or branched C1-C6-alkyl group or R5 and R6 and/or R5′ and R6′ taken together form an unsubstituted 4-7 membered ring condensed to the benzene ring of the indenyl moiety, and R7 and R7′ can be the same or are different and can be H or a linear or branched C1-C6-alkyl group (ii) an aluminoxane cocatalyst and/or (iii) a boron containing cocatalyst and (iv) optionally an aluminum alkyl compound.

Catalyst

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Page/Page column, (2014/07/08)

A catalyst comprising (i) an asymmetric complex of formula (I) wherein M is zirconium or hafnium; each X is a sigma ligand; L is a divalent bridge selected from -R'2C-, -R'2C-CR'2-, -R'2Si-, -R'2Si-SiR'2-, -R'2Ge-, wherein each R' is independently a hydrogen atom, C1-C20-alkyl, tri(C1-C20-alkyl)silyl, C6-C20-aryl, C7-C20-arylalkyl or C7-C20-alkylaryl; R2 and R2' are each independently linear C1-10 hydrocarbyl; R5 and R5' are each independently hydrogen or a C 1-20 hydrocarbyl group; R6 and R6' are each independently hydrogen or a C1-20 hydrocarbyl group; R7 is hydrogen or a C1-20 hydrocarbyl group or is ZR3; Z is O or S, preferably O; R3 is a C1-10 hydrocarbyl group; Ar is an aryl or heteroaryl group having up to 20 carbon atoms optionally substituted by one or more groups R8; Ar' is an aryl or heteroaryl group having up to 20 carbon atoms optionally substituted by one or more groups R8'; R8 and R8' are each independently is a C1-20 hydrocarbyl group; with the proviso that at least one of R6 or R7 is not H; and (ii) a cocatalyst comprising a compound of a group 13 metal, e.g. boron.

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