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Dichloro(N-methyl-N-phenylamino)borane, also known as [HN(C6H5)MeBH2Cl2], is a boron-based organometallic compound that features a boron atom bonded to two chlorine atoms, a methyl group, and a phenylamino group. Dichloro(N-methyl-N-phenylamino)borane is of interest in organic chemistry due to its potential applications as a reagent in various chemical transformations, such as in the reduction of carbonyl compounds to amines. The phenylamino group provides a sterically and electronically unique environment around the boron center, which can influence the reactivity and selectivity of the compound in chemical reactions. Its synthesis and use often involve controlled conditions to manage the reactivity of the boron center and the potential for side reactions. The compound's properties, such as its stability and solubility, can also be significant factors in its practical application in chemical synthesis.

1125-73-1

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1125-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1125-73-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1125-73:
(6*1)+(5*1)+(4*2)+(3*5)+(2*7)+(1*3)=51
51 % 10 = 1
So 1125-73-1 is a valid CAS Registry Number.

1125-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methylanilinoborane dichloride

1.2 Other means of identification

Product number -
Other names dichloro(N-methyanilino)borane

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:1125-73-1 SDS

1125-73-1Relevant academic research and scientific papers

Process for the production of o-(N-monosubstituted amino)benzyl alcohols

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, (2008/06/13)

Process for the production of o-(N-monosubstituted amino)benzyl alcohols which comprises reacting an N-mono-substituted aniline optionally having one or more substituents with a boron trihalogenide at a temperature from about 0° C. to about 100° C. and reacting the resultant boron compound with an aldehyde in the presence of a base at a temperature from about -30° C. to about 100° C. to regiospecifically introduce a 1-hydroxy-alkyl or 1-hydroxy-substituted alkyl group into the ortho position of said aniline.

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