Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1575-57-1

Post Buying Request

1575-57-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1575-57-1 Usage

General Description

2-oxobutyl acetate, also known as butyl acetoacetate, is a chemical compound with the molecular formula C6H10O3. It is a colorless liquid with a fruity, sweet odor and is commonly used as a solvent and in the production of various fragrances and flavorings. 2-oxobutyl acetate is also utilized in the manufacturing of paints, coatings, and adhesives due to its low volatility and good solvency properties. Additionally, it is employed as an intermediate in the synthesis of pharmaceuticals and other organic compounds. The chemical is considered to have low toxicity and is generally regarded as safe for use in consumer products when handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 1575-57-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1575-57:
(6*1)+(5*5)+(4*7)+(3*5)+(2*5)+(1*7)=91
91 % 10 = 1
So 1575-57-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O3/c1-3-6(8)4-9-5(2)7/h3-4H2,1-2H3

1575-57-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxobutyl acetate

1.2 Other means of identification

Product number -
Other names 1-Acetoxy-butan-2-on

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1575-57-1 SDS

1575-57-1Relevant articles and documents

Catalytic pyrolysis of cellulose in ionic liquid [bmim]OTf

Qu, Guangfei,He, Weiwei,Cai, Yingying,Huang, Xi,Ning, Ping

, p. 390 - 396 (2016/05/19)

This study discussed the catalytic cracking process of cellulose in ionic liquid 1-butyl-3-methylimidazolium trifluoromethanesulfonate ([bmim]OTF) under 180 °C, 240 °C and 340 °C, found that [bmim]OTF is an effective catalyst which can effectively reduce the pyrolysis temperature(nearly 200 °C) of the cellulose. FRIR, XRD and SEM were used to analyze the structure characterization of fiber before and after the cracking; GC-MS was used for liquid phase products analysis; GC was used to analyze gas phase products. The results showed that the cellulose pyrolysis in [bmim]OTf mainly generated CO2, CO and H2, also generated 2-furfuryl alcohol, 2,5-dimethyl-1,5-diallyl-3-alcohol, 1,4-butyrolactone, 5-methyl furfural, 4-hydroxy butyric acid, vinyl propionate, 1-acetoxyl group-2-butanone, furan formate tetrahydrofuran methyl ester liquid product, and thus simulated the evolution mechanism of cellulose pyrolysis products based on the basic model of cellulose monomer.

Direct and facile syntheses of heterocyclic vinyl-C-nucleosides for recognition of inverted base pairs by DNA triple helix formation: First report by direct Wittig route

Rothman, Jeffrey H.

, p. 3945 - 3948 (2008/02/01)

(Chemical Equation Presented) The ability to recognize specific gene sequences canonically would allow precise means for genetic intervention. However, specific recognition of two of the four possible base pairs by triplex-forming oligonucleotides (TFO) as X·T-A and Y·C-G within a triplex currently remains elusive. A series of C1-vinyl nucleosides have been proposed, and their stability and specificity have been evaluated extensively by molecular dynamics simulation. Because most C-nucleoside syntheses extend through direct substitution at the C1-position, a more convenient strategy for their syntheses via a direct Wittig coupling is presented here.

Gas-phase reaction of n-butyl acetate with the hydroxyl radical under simulated tropospheric conditions: Relative rate constant and product study

Veillerot,Foster,Guillermo,Galloo

, p. 235 - 243 (2007/10/03)

The gas-phase reaction of n-butyl acetate with hydroxyl radicals has been studied in an environmental smog chamber at 298 K. atmospheric pressure, and simulated tropospheric concentrations The rate constant for this reaction has been determined by a relative method and the experimental result, relative to n-octane used as reference compound, is k = 5.2 ± 0.5 × 10-12 cm3 molecule-1 s-1 This value appears to be about 25% higher than absolute rate constants found in the literature, but agrees very well with the other relative determination. Two reaction products have been identified and their production yield has been estimated, each accounting for about (15 ± 5)% of the overall OH reaction processes The two observed products are 2-oxobutyl acetate (CH3-CO-O-CH2-CO-CH2-CH3) and 3-oxobutyl acetate (CH3-CO-O-CH2-CH2-CO-CH3) The accuracy of the relative rate constant obtained is examined considering the evolution of the reactivity of the alkoxy end of the esters. Formation mechanisms for the two observed products are proposed and the likely other degradation channels are discussed

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1575-57-1