Structure

2,4-Dibromothiophene

CAS
3140-92-9
Catalog Number
ACM3140929
Category
Thiophenes
Molecular Weight
241.93
Molecular Formula
C4H2Br2S

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Specification

Synonyms
Thiophene, 2,4-dibromo-
Boiling Point
213.4 °C/760mmHg
Flash Point
82.9°C
Density
2.174 g/cm³ at 25 °C(lit.)
What is the molecular formula of 2,4-Dibromothiophene?

The molecular formula of 2,4-Dibromothiophene is C4H2Br2S.

What is the molecular weight of 2,4-Dibromothiophene?

The molecular weight of 2,4-Dibromothiophene is 241.93 g/mol.

When was 2,4-Dibromothiophene first created?

2,4-Dibromothiophene was first created on July 19, 2005.

What is the InChIKey of 2,4-Dibromothiophene?

The InChIKey of 2,4-Dibromothiophene is WAQFYSJKIRRXLP-UHFFFAOYSA-N.

How many hydrogen bond donor counts does 2,4-Dibromothiophene have?

2,4-Dibromothiophene has 0 hydrogen bond donor counts.

What is the topological polar surface area of 2,4-Dibromothiophene?

The topological polar surface area of 2,4-Dibromothiophene is 28.2 Å^2.

Is 2,4-Dibromothiophene a covalently-bonded unit?

Yes, 2,4-Dibromothiophene is a covalently-bonded unit.

How many heavy atoms are present in 2,4-Dibromothiophene?

There are 7 heavy atoms present in 2,4-Dibromothiophene.

What is the exact mass of 2,4-Dibromothiophene?

The exact mass of 2,4-Dibromothiophene is 241.82235 g/mol.

How many defined atom stereocenter counts does 2,4-Dibromothiophene have?

2,4-Dibromothiophene has 0 defined atom stereocenter counts.

Upstream Synthesis Route 1

  • 3141-24-0
  • 872-31-1
  • 3140-93-0
  • 3140-92-9

Reference: [1] Journal of Chemical Research - Part S, 1996, # 3, p. 150 - 151
[2] Organometallics, 2016, vol. 35, # 18, p. 3234 - 3239

Upstream Synthesis Route 2

  • 3141-24-0
  • 3140-93-0
  • 3140-92-9

Reference: [1] Justus Liebigs Annalen der Chemie, 1934, vol. 512, p. 136,156
[2] Justus Liebigs Annalen der Chemie, 1934, vol. 512, p. 136,156
[3] Organometallics, 2016, vol. 35, # 18, p. 3234 - 3239

Upstream Synthesis Route 3

  • 3141-24-0
  • 925-90-6
  • 3140-93-0
  • 3140-92-9

Reference: [1] Arkiv foer Kemi, 1958, vol. 12, p. 115,120

Downstream Synthesis Route 1

  • 3140-92-9
  • 109-72-8
  • 60-29-7
  • 15719-64-9
  • 16694-18-1

Reference: [1]Arkiv foer Kemi,1957,vol. 11,p. 317,322
[2]Arkiv foer Kemi,1957,vol. 11,p. 317,322

Downstream Synthesis Route 2

  • 3140-92-9
  • 16694-18-1

Reference: [1]Arkiv foer Kemi,1957,vol. 11,p. 317,322
[2]Arkiv foer Kemi,1957,vol. 11,p. 317,322

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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