BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE

ChemicalBook > CAS DataBase List > BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE

BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE

Product Name: BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE
CAS No.: 38857-88-4
Chemical Name: BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE
Synonyms: Bis(2,2,2-trichloroethyl) azodicarboxyle;BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE;Bis(2,2,2-trichloroethyl) azodicarboxylate;BEAZ Bis(2,2,2-trichloroethyl) azodicarboxylate;BIS(2,2,2-TRICHLOROETHYL) AZODI-CARBOXYL ATE, 97+%;AZODICARBOXYLIC ACID BIS(2,2,2-TRICHLOROETHYL) ESTER;1,2-Diazenedicarboxylic acid, 1,2-bis(2,2,2-trichloroethyl) ester
CBNumber: CB2149725
Molecular Formula: C6H4Cl6N2O4
Formula Weight: 380.83
MOL File: 38857-88-4.mol

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BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE Property

Melting point:: 109-111 °C (lit.)
Boiling point:: 380.7±42.0 °C(Predicted)
Density: 1.78±0.1 g/cm3(Predicted)
storage temp.: 2-8°C
solubility: sol in a wide range of organic solvents.
form: solid
color: slightly yellow
BRN: 2141527
CAS DataBase Reference: 38857-88-4

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Safety

Hazard Codes: Xi
Risk Statements: 36/37/38
Safety Statements: 26-36
WGK Germany: 3

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 291536
Product name: Bis(2,2,2-trichloroethyl) azodicarboxylate
Purity: ≥97%
Packaging: 5g
Price: $209
Updated: 2023/01/07

TRC

Product number: B119293
Product name: BEAZBis(2,2,2-trichloroethyl)azodicarboxylate
Packaging: 100mg
Price: $60
Updated: 2021/12/16

TRC

Product number: B119293
Product name: BEAZBis(2,2,2-trichloroethyl)azodicarboxylate
Packaging: 500mg
Price: $110
Updated: 2021/12/16

Biosynth Carbosynth

Product number: FB01254
Product name: Bis(2,2,2-trichloroethyl) azodicarboxylate
Packaging: 5G
Price: $135
Updated: 2021/12/16

Biosynth Carbosynth

Product number: FB01254
Product name: Bis(2,2,2-trichloroethyl) azodicarboxylate
Packaging: 2g
Price: $60
Updated: 2021/12/16

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BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE Chemical Properties,Usage,Production

Chemical Properties

Yellow powder or crystals

Uses

Bis(2,2,2-trichloroethyl) azodicarboxylate has been used:

in the asymmetric synthesis of substituted cycloalkyl[b]indoles
as amination reagent during the aza-ene reaction of different alkenes to yield the corresponding allyl amines
in para-directed amination of C₂-alkyl substituted anisole
in the synthesis of acid- and base-sensitive azo compounds and in Diels-Alder cycloadditions

General Description

Thermal inverse-type hetero-Diels-Alder reaction of O-silyl-protected lactal and bis(2,2,2-trichloroethyl) azodicarboxylate has been reported.

storage

Bis(2,2,2-trichloroethyl) azodicarboxylate is same as with all azo compounds, caution should be exercised to avoid exposure of the material to heat. Store in a brown bottle.

BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE Preparation Products And Raw materials

Raw materials

Preparation Products

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BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE Suppliers

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38857-88-4, BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATERelated Search:

AZODICARBOXYLIC ACID DIMETHYL ESTER 1,1,1-Trichloroethane BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE Chloroform Diethyl azodicarboxylate Trichloroethanol AMMONIUM CARBAMATE 4-METHOXYBENZENESULFONAMIDE

BIS(2,2,2-TRICHLOROETHYL) AZODI-CARBOXYL ATE, 97+%

AZODICARBOXYLIC ACID BIS(2,2,2-TRICHLOROETHYL) ESTER

BIS(2,2,2-TRICHLOROETHYL) AZODICARBOXYLATE

Bis(2,2,2-trichloroethyl) azodicarboxyle

BEAZ Bis(2,2,2-trichloroethyl) azodicarboxylate

1,2-Diazenedicarboxylic acid, 1,2-bis(2,2,2-trichloroethyl) ester

Bis(2,2,2-<WBR>trichloroethyl) azodicarboxylate

38857-88-4

C6H4Cl6N2O

C6H4Cl6N2O4

CCl3CH2OCONNCOOCH2CCl3

Building Blocks

Azo/Diazo Compounds

C-X Bond Formation (Non-Halogen)

Mitsunobu

Organic Building Blocks

Nitrogen Compounds

Synthetic Reagents