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Chloro(N,N-dimethylmethanamine)dihydridoboron, also known as chloro(N,N-dimethylmethylamine)dihydridoboron or [HB(NMe2)2Cl], is a chemical compound consisting of a boron atom bonded to two hydride (H) ligands, a chloro (Cl) ligand, and an N,N-dimethylmethanamine (NMe2) ligand. This organoboron compound is a derivative of borane (BH3), where one of the hydride ligands is replaced by the N,N-dimethylmethanamine group. It is a colorless, volatile liquid with a pungent odor and is sensitive to air and moisture. Chloro(N,N-dimethylmethanamine)dihydridoboron is used as a reagent in organic synthesis, particularly in the formation of carbon-boron bonds and as a reducing agent. It is also employed in the synthesis of various organoboron compounds and as a catalyst in certain chemical reactions. Due to its reactivity, it is typically handled under an inert atmosphere and stored away from light and heat.

5353-44-6

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5353-44-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5353-44-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5353-44:
(6*5)+(5*3)+(4*5)+(3*3)+(2*4)+(1*4)=86
86 % 10 = 6
So 5353-44-6 is a valid CAS Registry Number.

5353-44-6SDS

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 [chloromethyl(dimethyl)azaniumyl]boron

1.2 Other means of identification

Product number -
Other names chloro-dihydrido-trimethylammonio-boron

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:5353-44-6 SDS

5353-44-6Relevant academic research and scientific papers

Formation of amine, phosphine, and thioether adducts of chlorotriborane(7)

Dodds, Alan R.,Nelson, Mansel A.,Kodama, Goji

, p. 4517 - 4521 (2008/10/08)

The chlorotriborane(7) (B3H6Cl) adduct of N(CH3)3 was formed by the reaction of B4H8·N(CH3)3 with HCl in dichloromethane or with HgCl2 in chloroform. The reaction of B3H7·N(CH3)3 with BCl3 in dichloromethane was found to be a better preparative method for B3H6Cl·N(CH3)3. The BCl3 treatment was employed to convert the N(CH3)2H, N(CH3)H2, NH3, and S(CH3)2 adducts of B3H7 into the corresponding adducts of B3H6Cl. In contrast, B3H7·P(CH3)3 and B3H7·PH3 are inert to BCl3. The B3H6Cl adducts of P(CH3)3 and PH3 could be obtained by treating the B3H7 adducts with a mixture of HCl and BCl3 in dichloromethane. The 11B and 1H NMR spectra of these B3H6Cl adducts showed that their structures were described as 1-(Lewis base)-2-chlorotriborane(7).

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