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10388-28-0

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10388-28-0 Usage

General Description

Chloroborane, with the chemical formula BCl3, is a colorless, toxic gas with a pungent, irritating odor. It is a boron-halogen compound that is used in organic synthesis as a catalyst for various reactions, such as polymerization and isomerization. Chloroborane is highly reactive and can react violently with water, alcohols, and other organic compounds. It is also used in the production of boron nitride and boron carbide. Due to its toxic and corrosive nature, proper handling and use of chloroborane are necessary to avoid harmful exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 10388-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,8 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10388-28:
(7*1)+(6*0)+(5*3)+(4*8)+(3*8)+(2*2)+(1*8)=90
90 % 10 = 0
So 10388-28-0 is a valid CAS Registry Number.
InChI:InChI=1/BCl/c1-2

10388-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name chloroboron

1.2 Other means of identification

Product number -
Other names monochloroborane

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:10388-28-0 SDS

10388-28-0Relevant articles and documents

Chemistry of Dimetallaboranes Derived from the Reaction of [Cp*MCl2]2 with Monoboranes (M = Ru, Rh; Cp* = η5-C5Me5)

Lei, Xinjian,Shang, Maoyu,Fehlner, Thomas P.

, p. 1275 - 1287 (1999)

In a single step, from [Cp*RuCl2]2 (Cp* = η5-C5Me5) and Li[BH4], nido-1,2-(Cp*Ru)2(μ-H)2B3H 7, 1, is produced in high yield. Addition of BH3·THF to 1 results in conversion to nido-1,2-(Cp*Ru)2(μ-H)B4H9, 2. Reaction of BH3·THF directly with [Cp*RuCl2]2 yields a mixture of 1 and 2. In two steps, a rhodium analogue, nido-2,3-(Cp*Rh)2B3H7, 9, is accessible by the reaction of [Cp*RhCl2]2 and Li[BH4] to exclusively produce (Cp*Rh)2B2H6, 8, which adds BH3·THF to give 9 as the major product in a mixture. Reaction of BH3·THF directly with [Cp*RhCl2]2 yields the chloro derivative of 9, nido-1-Cl-2,3-(Cp*Rh)2B3H6, 11, in high yield via the intermediate positional isomer, nido-3-Cl-1,2-(Cp*Rh)2B3H6, 10. With high concentrations of Co2(CO)8, 1 reacts with Co2(CO)8 to give nido-1-(Cp*Ru)-2-(Cp*RuCO)-3-Co(CO)2(μ 3-CO)B3H6,3, whereas low concentrations permit competitive degradation of 1 to yield arachno-(Cp*Ru)(CO)(μ-H)B3H7, 4. On the other hand, reaction of 11 with Co2(CO)8 gives closo-1-Cl-6-{Co(CO)2}-2,3-(Cp*Rh)2(μ 3-CO)B3H3, 12. Mild thermolysis of 3 results in loss of hydrogen and the formation of closo-6-Co(CO)2-2,3-(Cp*Ru)2(μ-CO)(μ 3-CO)B3H4, 5, whereas thermolysis of 2 results in loss of hydrogen and formation of pileo-2,3-(Cp*Ru)2B4H8, 6, with a BH-capped square pyramidal structure. Finally, 6 reacts with Fe2(CO)9 to yield pileo-6-Fe(CO)3-2,3-(Cp*Ru)2(μ 3-CO)B4H4, 7, with a BH-capped octahedral cluster structure. The overall isolated yield of 7, formed in four steps from [Cp*RuCl2]2, is ≈50% and evidences good control of reactivity.

The Reaction of cis-1,2-Dichloroethylene with Borane in Tetrahydrofuran. The Supply of Monochloroborane in Tetrahydrofuran Solution

Arase, Akira,Hoshi, Masayuki,Masuda, Yuzuru

, p. 299 - 300 (1981)

In the reaction of cis-1,2-dichloroethylene with borane in THF at 20 deg C for 2 h, about 94percent of borane was converted to monochloroborane.The resulting solution was stable at 0 deg C for several hours.

The interaction of boron trichloride with diborane

Kerrigan, James V.

, p. 908 - 910 (2008/10/08)

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