CAS 21860-03-7

2,5-di-tert-butylaniline

Description:

2,5-Di-tert-butylaniline is an organic compound characterized by its structure, which features two tert-butyl groups attached to the aniline moiety at the 2 and 5 positions of the benzene ring. This compound is a derivative of aniline, where the amino group (-NH2) is bonded to a benzene ring, and the presence of bulky tert-butyl groups enhances its steric hindrance and lipophilicity. It is typically a solid at room temperature and is known for its low solubility in water due to the hydrophobic nature of the tert-butyl groups. 2,5-Di-tert-butylaniline is used in various applications, including as an intermediate in the synthesis of dyes, pigments, and other organic compounds. Additionally, it may exhibit interesting properties such as thermal stability and resistance to oxidation, making it valuable in certain industrial processes. Safety data should be consulted, as with any chemical, to understand its handling, storage, and potential hazards.

Formula: C₁₄H₂₃N

InChI: InChI=1/C14H23N/c1-13(2,3)10-7-8-11(12(15)9-10)14(4,5)6/h7-9H,15H2,1-6H3

SMILES: CC(C)(C)c1ccc(c(c1)N)C(C)(C)C

2,5-Di-tert-butylaniline

CAS: 21860-03-7

Formula: C₁₄H₂₃N

Purity: 95%

Color and Shape: Solid

Molecular weight: 205.3391

Ref: IN-DA003G15

2,5-Di-Tert-Butylaniline

CAS: 21860-03-7

2,5-Di-Tert-Butylaniline

Purity: 99%

Molecular weight: 205.34g/mol

Ref: 54-OR1010116

2,5-Di-tert-butylaniline

CAS: 21860-03-7

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Formula: C₁₄H₂₃N

Purity: Min. 99 Area-%

Molecular weight: 205.34 g/mol

Ref: 3D-J-014317

2,5-Di-tert-butylaniline

CAS: 21860-03-7

Purity: 95%

Molecular weight: 205.3450012

Ref: 10-F603944

2,5-Di-tert-butylaniline

CAS: 21860-03-7

2,5-Di-tert-butylaniline is a chlorinating agent that reacts with DNA to form thymine lesion. This lesion can be repaired by the action of thymine glycol, which converts a T to a C. The chlorination of DNA can induce cancer cell death and has been shown to inhibit the growth of tumor cells in vitro. 2,5-Di-tert-butylaniline is also known to react with amines, including phenoxy groups and xanthine. These reactions are thought to be responsible for its carcinogenic effects.

Formula: C₁₄H₂₃N

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 205.34 g/mol

Ref: 3D-FD174861