CAS 1694-31-1

Acetoacetato di tert-butile

Descrizione:

Acetoacetato di tert-butile, con il numero CAS 1694-31-1, è un composto organico caratterizzato dal suo gruppo funzionale estere. È un liquido incolore a giallo pallido con un odore fruttato, comunemente usato come reagente nella sintesi organica e come intermediario nella produzione di prodotti farmaceutici e agrochimici. Il composto presenta un gruppo tert-butile, che contribuisce al suo ingombro sterico e influenza la sua reattività. Acetoacetato di tert-butile è solubile in solventi organici come etanolo ed etere, ma ha una solubilità limitata in acqua a causa del suo gruppo tert-butile idrofobico. È noto per la sua capacità di subire varie reazioni chimiche, tra cui condensazione e acilazione, rendendolo prezioso nella chimica organica sintetica. Inoltre, ha un profilo di tossicità relativamente basso, ma devono essere osservate le precauzioni di sicurezza standard quando lo si maneggia, come con qualsiasi sostanza chimica. In generale, Acetoacetato di tert-butile è un composto versatile con applicazioni significative nella sintesi chimica.

Formula: C₈H₁₄O₃

InChI: InChI=1S/C8H14O3/c1-6(9)5-7(10)11-8(2,3)4/h5H2,1-4H3

InChI key: InChIKey=JKUYRAMKJLMYLO-UHFFFAOYSA-N

SMILES: O(C(C)(C)C)C(CC(C)=O)=O

Sinonimi:

• 1,1-Dimethylethyl 3-oxobutanoate
• 1,1-Dimethylethyl acetoacetate
• 3-Oxobutanoate de 1,1-dimethylethyle
• 3-Oxobutanoic acid 1,1-dimethylethyl ester
• 3-Oxobutyric acid tert-butyl ester
• Acetessigsaure-tert-butylester
• Acetoacetate, Tert-Butyl
• Acetoacetic acid tert-butyl ester
• Acide butanoique, oxo-3-, ester de dimethylethyle-1,1
• Butanoic acid, 3-oxo-, 1,1-dimethylester
• Butansaure, 3-oxo-, 1,1-dimethylethylester
• Lonza TBAA
• Nsc 42869
• Tert-Butyl Acetoacetate
• t-Butyl acetoacetate
• tert-Butyl 3-oxobutanoate
• tert-Butyl 3-oxobutyrate
• tert-Butyl acetylacetate
• tert-Butyl acetylacetonate

tert-Butyl Acetoacetate

CAS: 1694-31-1

Formula: C₈H₁₄O₃

Purezza: >95.0%(GC)

Colore e forma: Colorless to Almost colorless clear liquid

Peso molecolare: 158.20

Ref: 3B-A0816

tert-Butyl acetoacetate, 97%

CAS: 1694-31-1

tert-Butyl acetoacetate is used as intermediate for the syntheses of different organic chemicals. Raw material in pharmaceutical Industry, In agrochemical industry. Reagent for Acyloin synthesis and ?, - unsaturated ketones synthesis. This Thermo Scientific Chemicals brand product was originally par

Formula: C₈H₁₄O₃

Purezza: 97%

Colore e forma: Clear colorless to yellow, Liquid

Peso molecolare: 158.20

Ref: 02-A11115

tert-Butyl acetoacetate

CAS: 1694-31-1

Formula: C₈H₁₄O₃

Purezza: 97%

Colore e forma: Liquid

Peso molecolare: 158.1950

Ref: IN-DA0035N1

tert-Butyl acetoacetate

CAS: 1694-31-1

tert-Butyl acetoacetate

Purezza: 98%

Peso molecolare: 158.20g/mol

Ref: 54-OR75213

tert-Butyl acetoacetate

CAS: 1694-31-1

Formula: C₈H₁₄O₃

Peso molecolare: 158.20

Ref: 7W-GK2330

tert-Butyl 3-oxobutanoate

CAS: 1694-31-1

Formula: C₈H₁₄O₃

Purezza: 95%

Colore e forma: Liquid

Peso molecolare: 158.197

Ref: 10-F235667

tert-Butyl Oxobutyrate

Prodotto controllato

CAS: 1694-31-1

Applications tert-Butyl Oxobutyrate is a chemical reagent used in the preparation of a potent Bcl-2/Bcl-xL inhibitor used in tumor inhibition. Also used in the synthesis of potent small molecule-peptide conjugates in HIV-1 inhibition.
References Aguilar, A. et al.: J. Med. CHem., 56, 3048 (2013); Wang, C. et al.: J. Med. Chem., 56, 2527

Formula: C₈H₁₄O₃

Colore e forma: Neat

Peso molecolare: 158.19

Ref: TR-B693435

tert-Butyl acetoacetate

CAS: 1694-31-1

tert-Butyl acetoacetate is an organic molecule that contains nitrogen atoms. The structure of tert-butyl acetoacetate can be described as a planar molecule with two hydrogen atoms and two carbon atoms. One of the hydrogen atoms is bonded to the carbon atom in the middle, and the other hydrogen atom is bonded to one of the carbons on the outside. The compound has a coordination geometry with a sodium ion in its center, and it can also exist as an anion or as a cation. Tert-butyl acetoacetate was synthesized by reacting sodium carbonate with tert-butyl alcohol. This reaction is exothermic and produces tert-butyl acetoacetate along with water and sodium hydroxide. In addition, tert-butyl acetoacetate is toxicologically studied, which has shown that it does not have any carcinogenic effects or adverse effects on reproduction in rats at doses up to 2000 mg/kg/day

Formula: C₈H₁₄O₃

Purezza: Min. 95%

Peso molecolare: 158.19 g/mol

Ref: 3D-FB01780