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Tribromoacetaldehyde

Tribromoacetaldehyde structure

Tribromoacetaldehyde 

structure
  • CAS No:

    115-17-3

  • Formula:

    C2HBr3O

  • Chemical Name:

    Tribromoacetaldehyde

  • Synonyms:

    Acetaldehyde,2,2,2-tribromo-;Bromal;Acetaldehyde,tribromo-;2,2,2-Tribromoacetaldehyde;Tribromoacetaldehyde;NSC 66406;2,2,2-Tribromoethanal;29986-20-7

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

Oily, yellowish liquid. Soluble in water, alcohol, or ether. Combustible.

Tribromoacetaldehyde Basic Attributes

280.74

280.74

204-067-9

W2WDI7648E

66406

DTXSID1021667

YELLOWISH, OILY LIQUID

29130000

Characteristics

17.1

3.17

2.66 g/cm3

-57.5 °C

174 °C

150 °F

n 20/D 1.584(lit.)

SOL IN ACETONE

Refrigerator (+4°C)

1.52 mmHg

FORMS WITH WATER BROMAL HYDRATE WHICH IS SOLID @ TEMP BELOW 50 °C|MONOCLINIC PRISMS (OBTAINED FROM WATER CRYSTALLIZING WITH 1 MOLECULE OF SOLVENT/MOLECULE COMPD)

Safety Information

III

8

UN 2927 6.1/PG 1

3

25-27-34

26-28-36/37/39-45-28A

AB3237500

T+,Xi,T

Irritant

P280-P302 + P350-P305 + P351 + P338-P310

H301-H310-H314

|Danger|H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]|P260, P262, P264, P270, P280, P301+P310, P301+P330+P331, P302+P350, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P322, P330, P361, P363, P405, and P501|Aggregated GHS information provided by 39 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

IN PATIENTS SUFFERING FROM CHRONIC INTOXICATION, GASTRITIS IS COMMON & SKIN ERUPTIONS MAY DEVELOP. PARENCHYMATOUS RENAL INJURY MAY ALSO OCCUR. /CHLORAL HYDRATE/|IRRITANT ACTIONS OF CHLORAL HYDRATE GIVE RISE TO UNPLEASANT TASTE...NAUSEA, OCCASIONAL VOMITING, & FLATULENCE. ... UNDESIRABLE CNS EFFECTS INCL LIGHT-HEADEDNESS, MALAISE, ATAXIA, & NIGHTMARES. /CHLORAL HYDRATE/

2,2,2-tribromoacetaldehyde

Tribromoacetaldehyde Use and Manufacturing

Methods of Manufacturing

It can be obtained by the reaction of ethanol and bromine; or it can be obtained by the reaction of trichloroacetaldehyde and bromine; it can also be obtained by the reaction of triacetaldehyde and bromine. 69 g of dry triacetaldehyde was dropped into a mixture of 720 g of bromine and 1.5 g of sulfur, and the reaction proceeded under its own exotherm. Then it was heated at 60-80°C for 2h, and the crude product collected by distillation was distilled under reduced pressure again, and a fraction of 71-74°C (2.4kPa) was taken to obtain 220-240g of bromoaldehyde.

Uses

Organic synthesis.

Acetaldehyde, 2,2,2-tribromo-: INACTIVE

Computed Properties

Molecular Weight:280.74
XLogP3:2.1
Hydrogen Bond Acceptor Count:1
Exact Mass:279.75570
Monoisotopic Mass:277.75775
Topological Polar Surface Area:17.1
Heavy Atom Count:6
Complexity:54.3
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Material

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