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1,2-dimethylborane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 17156-88-6 Structure
  • Basic information

    1. Product Name: 1,2-dimethylborane
    2. Synonyms: 1,2-dimethylborane
    3. CAS NO:17156-88-6
    4. Molecular Formula: C2H10B2
    5. Molecular Weight: 55.724
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17156-88-6.mol
  • Chemical Properties

    1. Melting Point: -125°C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /liquid
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,2-dimethylborane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-dimethylborane(17156-88-6)
    11. EPA Substance Registry System: 1,2-dimethylborane(17156-88-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. RIDADR: 1953
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: 2.3
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 17156-88-6(Hazardous Substances Data)

17156-88-6 Usage

Physical state

Colorless, flammable gas

Odor

Pungent, fishy

Primary use

Research chemical in organic synthesis

Secondary use

Reagent in various chemical reactions

Additional use

Fuel for certain rockets and jet engines

Energy content

High

Toxicity

Highly toxic

Handling precautions

Must be handled with extreme caution

Reactivity

Highly reactive

Hazard

Can spontaneously ignite in air

Applications

Industrial and scientific

Safety concerns

Dangerous to handle due to toxicity and reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 17156-88-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,5 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17156-88:
(7*1)+(6*7)+(5*1)+(4*5)+(3*6)+(2*8)+(1*8)=116
116 % 10 = 6
So 17156-88-6 is a valid CAS Registry Number.

17156-88-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyldiborane

1.2 Other means of identification

Product number -
Other names 1.2-(CH3)2B2H4

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:17156-88-6 SDS

17156-88-6Relevant articles and documents

Dimethylindium octahydrotriborate, Me2InB3H8: Synthesis, crystal structure and spectroscopic properties of a volatile indium hydride

Aldridge, Simon,Downs, Anthony J.,Parsons, Simon

, p. 2055 - 2056 (2007/10/03)

Reaction between trimethylindium and tetraborane(10) at room temperature yields the volatile, viscous liquid dimethylindium octahydrotriborate, the first reported example of a volatile indium hydride; spectroscopic properties of the vapour indicate a molecular structure akin to that of Me2AlB3H8, although the crystal structure implies a more ionic formulation, [Me2In]+[B3H8]-, with the coordination at each indium centre being augmented via secondary intermolecular interactions with terminal hydrogen atoms.

Dealkylation of Zirconium(IV) by Borane: The Intimate Mechanism of an Alkyl Transfer Reaction

Marsella, John A.,Caulton, Kenneth G.

, p. 2361 - 2365 (2007/10/02)

The reaction of Cp2ZrMe2 with BH3*THF ultimately yields Cp2Zr(BH4)2.The reaction is sequential in the sense that Cp2Zr(BH4)Me has also been detected.By use of 11B NMR spectroscopy, both for resolution of chemically distinct boron-containing species and as an aid to proton counting, it has been possible to show that these reactions proceed through intermediates containing coordinated BH3Me- and BH2Me2-, and thus the reaction is initially a formal insertion of BH3 into a Zr-CH3 bond.These intermediates react further with borane to produce a complex equilibrating mixture of alkyl diboranes, B2MenH6-n and Zr(BH4) groups.

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