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Trans-1,4-Dibromo-2-butene is a synthetic, organic compound that belongs to the family of bromoalkenes. It is composed of carbon, hydrogen, and bromine atoms, with the chemical formula C4H6Br2. TRANS-1,4-DIBROMO-2-BUTENE is known to pose potential health hazards, as it may be harmful if inhaled, swallowed, or come in contact with the skin.

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  • 6974-12-5 Structure
  • Basic information

    1. Product Name: TRANS-1,4-DIBROMO-2-BUTENE
    2. Synonyms: TRANS-1,4-DIBROMOBUT-2-ENE;1,4-DIBROMO-2-BUTENE;1,4-dibromo-2-buten;TL 80;tl80;1,4-dibromobut-2-ene;Cis-1,4-DibromoButene;2-Butene, 1,4-dibromo-
    3. CAS NO:6974-12-5
    4. Molecular Formula: C4H6Br2
    5. Molecular Weight: 213.9
    6. EINECS: 212-472-7
    7. Product Categories: N/A
    8. Mol File: 6974-12-5.mol
  • Chemical Properties

    1. Melting Point: 48-51 °C(lit.)
    2. Boiling Point: 205 °C(lit.)
    3. Flash Point: 113 °C
    4. Appearance: colorless to slightly brown/
    5. Density: 1.9393 (estimate)
    6. Vapor Pressure: 0.405mmHg at 25°C
    7. Refractive Index: 1.5430 (estimate)
    8. Storage Temp.: 0-6°C
    9. Solubility: N/A
    10. CAS DataBase Reference: TRANS-1,4-DIBROMO-2-BUTENE(CAS DataBase Reference)
    11. NIST Chemistry Reference: TRANS-1,4-DIBROMO-2-BUTENE(6974-12-5)
    12. EPA Substance Registry System: TRANS-1,4-DIBROMO-2-BUTENE(6974-12-5)
  • Safety Data

    1. Hazard Codes: T
    2. Statements: 25-34
    3. Safety Statements: 26-36/37/39-45
    4. RIDADR: UN 2923 8/PG 2
    5. WGK Germany: 2
    6. RTECS: EM4725000
    7. F: 8-19
    8. HazardClass: N/A
    9. PackingGroup: N/A
    10. Hazardous Substances Data: 6974-12-5(Hazardous Substances Data)

6974-12-5 Usage

Uses

Used in Chemical Industry:
Trans-1,4-Dibromo-2-butene is used as an intermediate in the synthesis of other chemicals, contributing to the production of various chemical products.
Used in Laboratory Research:
Trans-1,4-Dibromo-2-butene is employed as a reagent or starting material in laboratory research settings, where it is utilized for the development and testing of new chemical compounds and processes.

Check Digit Verification of cas no

The CAS Registry Mumber 6974-12-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6974-12:
(6*6)+(5*9)+(4*7)+(3*4)+(2*1)+(1*2)=125
125 % 10 = 5
So 6974-12-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H6Br2/c5-3-1-2-4-6/h1-2H,3-4H2/b2-1-

6974-12-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name TRANS-1,4-DIBROMO-2-BUTENE

1.2 Other means of identification

Product number -
Other names Cis-1,4-DibromoButene

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:6974-12-5 SDS

6974-12-5Relevant articles and documents

Fourth subgroup metal complex with rigid annular bridging structure and application of fourth subgroup metal complex

-

Paragraph 0058; 0061; 0067, (2021/06/23)

The invention belongs to the technical field of olefin polymerization catalysts, and particularly relates to a fourth subgroup metal complex with a rigid annular bridging structure and an application of the fourth subgroup metal complex. The fourth subgroup metal complex provided by the invention has a structure represented by a formula (A) or a formula (B), X is halogen or alkyl; and M is titanium, zirconium or hafnium. On the basis of a non-metallocene catalyst, a bridging structure in catalyst molecules is improved and upgraded, and a brand-new metal complex with excellent catalytic performance and good high-temperature tolerance is designed; when the fourth subgroup metal complex is used as a main catalyst to catalyze olefin polymerization reaction, under the activation action of a small amount of mixed cocatalyst, the fourth subgroup metal complex can efficiently catalyze the copolymerization reaction of ethylene and alpha-olefin to obtain polyolefin with high molecular weight and high comonomer insertion rate.

Batchwise and continuous organophilic nanofiltration of Grubbs-type olefin metathesis catalysts

Schoeps, Dirk,Buhr, Kristian,Dijkstra, Marga,Ebert, Katrin,Plenio, Herbert

experimental part, p. 2960 - 2965 (2009/12/08)

A mass-tagged N-mesityl imidazolinium salt with four additional -CH 2NCy2 substituents was synthesized, leading to a molecular mass of nearly 1100 g mol-1 in the corresponding carbene ligand. This mass-tagged ligand was used to generate the respective Grubbs II and Grubbs-Hoveyda type complexes. The catalytic activity of the latter complex was tested in several olefin metathesis reactions and found to be slightly superior to that of the related N-mesityl based complex. In batchwise solvent resistant nanofiltration experiments the ruthenium complex dissolved in toluene and following a metathesis reactions was efficiently retained (>99.8%) by a single nanofiltration; the permeate contained less than 4 ppm of Ru. Equally efficient catalyst retention was observed in a membrane reactor utilized for the continuous synthesis of a RCM product.

Cross-metathesis of vinylsilanes carrying electron-withdrawing substituents with olefins in the presence of the second-generation Grubbs catalyst

Pietraszuk, Cezary,Marciniec, Bogdan,Fischer, Helmut

, p. 7121 - 7124 (2007/10/03)

The efficient cross-metathesis of vinylsilanes carrying electron-withdrawing substituents with various olefins is described. High yields and selectivities were obtained when styrene, 1-hexene, and selective functional allyl derivatives were used as the ol

Efficient procedures for 1-bromo-1,3-butadiene and 2-bromo-1,3-butadiene

Keegstra,Verkruijsse,Andringa,Brandsma

, p. 721 - 726 (2007/10/02)

Mixtures of Z- and E-1-bromo-1,3-butadiene in which the E- or Z- isomer predominates have been obtained in good yields by treating a mixture of Z- and E-1,4-dibromo-2-butene (90% Z-isomer) or pure E-1,4-dibromo-2-butene, respectively, with powdered potassium hydroxide in high-boiling petroleum. 2-Bromo-1,3-butadiene was obtained in high yields by stirring a mixture of vinylacetylene, concentrated aqueous hydrogen bromide and copper(I) bromide.

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