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(Dimethyl sulfide)trihydroboron

(Dimethyl sulfide)trihydroboron structure

(Dimethyl sulfide)trihydroboron 

structure
  • CAS No:

    13292-87-0

  • Formula:

    C2H9BS

  • Chemical Name:

    (Dimethyl sulfide)trihydroboron

  • Synonyms:

    Boron,trihydro[thiobis[methane]]-,(T-4)-;Methyl sulfide,compd. with borane (1:1);Borane,compd. with thiobis[methane] (1:1);Methyl sulfide,compd. with BH3;Borine,compd. with Me2S;Borane,compd. with methyl sulfide (1:1);Methane,thiobis-,compd. with borane (1:1);Methane,thiobis-,boron complex;(T-4)-Trihydro[thiobis[methane]]boron;Dimethylsulfane compd. with borane (1:1);BMS;Borane-dimethyl sulfide (1:1);Borane-dimethyl sulfide complex (1:1);(Dimethyl sulfide)borane;(Dimethyl sulfide)trihydroboron;Trihydrido(dimethyl sulfide)boron;Trihydro(dimethyl sulfide)boron;Borane-dimethylsulfide complex;Dimethylsulfide trihydroborane;12070-92-7;153096-90-3;163858-17-1;168641-59-6;172146-69-9;664339-46-2;856617-77-1;1037067-65-4;1262951-71-2;1315334-90-7;1628073-40-4

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

clear colorless to light yellow solution

(Dimethyl sulfide)trihydroboron Basic Attributes

75.97

76.051804

3663489

236-313-6

DTXSID3051672

29309090

Characteristics

25.3

-0.47240

Colorless to pale yellow Solution

1.287 g/mL at 25 °C

-40--37°C

~34 °C

65 °F

1.457

Solubility in water: reaction.Miscible with ethyl ether, tetrahydrofurane, dichloromethane, benzene, xylene, hexane, diglyme, dimethyl ether, ethyl acetate, toluene, methylene chloride and other aprotic solvents.

2-8°C

Safety Information

II

4.3

UN 3399 4.3/PG 1

3

12-14/15-19-20/22-37/38-41-67-65-63-48/20-38-11-22-14-40-36-21-36/37/38-37

36/37-62-36/39-33-26-23-16-36-24/25-7/8-43-39-36/37/39

PV5080000

F+,Xn,F,Xi

P210-P223-P231 + P232-P280-P370 + P378-P422

H225-H260-H302-H318

|Danger|H225 (95.71%): Highly Flammable liquid and vapor [Danger Flammable liquids]|P201, P202, P210, P223, P231+P232, P233, P240, P241, P242, P243, P261, P264, P270, P271, P273, P280, P281, P301+P310, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P308+P313, P310, P312, P321, P322, P330, P332+P313, P335+P334, P361, P362, P363, P370+P378, P402+P404, P403+P233, P403+P235, P405, and P501|Aggregated GHS information provided by 164 companies from 16 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

(Dimethyl sulfide)trihydroboron Use and Manufacturing

Uses

It is used in the asymmetric reduction of indone and tetralone with L-pyrrolidone supported by dendrimer. The conversion of ferrocenyl-1,3-dione to chiral 1,3-diol is catalyzed by CBS asymmetric reduction. Highly asymmetric reduction of ketone catalyzed by C3-symmetric three-legged hydroxylamide. The reactant is used as a specifically selected reducing agent.The reactant participates in: Hydroboration/synthesis of cage compounds.

Boron, trihydro[thiobis[methane]]-, (T-4)-: ACTIVE

Computed Properties

Molecular Weight:72.95
Hydrogen Bond Acceptor Count:1
Exact Mass:73.0283265
Monoisotopic Mass:73.0283265
Topological Polar Surface Area:25.3
Heavy Atom Count:4
Complexity:2.8
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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