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4-BUTOXY-2-BUTANONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 30536-44-8 Structure
  • Basic information

    1. Product Name: 4-BUTOXY-2-BUTANONE
    2. Synonyms: 4-BUTOXY-2-BUTANONE;4-Butoxybutane-2-one;5-Oxanonane-2-one
    3. CAS NO:30536-44-8
    4. Molecular Formula: C8H16O2
    5. Molecular Weight: 144.21144
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 30536-44-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 180-181 °C(Press: 676 Torr)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.8893 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-BUTOXY-2-BUTANONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-BUTOXY-2-BUTANONE(30536-44-8)
    11. EPA Substance Registry System: 4-BUTOXY-2-BUTANONE(30536-44-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 30536-44-8(Hazardous Substances Data)

30536-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30536-44-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,5,3 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 30536-44:
(7*3)+(6*0)+(5*5)+(4*3)+(3*6)+(2*4)+(1*4)=88
88 % 10 = 8
So 30536-44-8 is a valid CAS Registry Number.

30536-44-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-butoxybutan-2-one

1.2 Other means of identification

Product number -
Other names InChI=1/C8H16O2/c1-3-4-6-10-7-5-8(2)9/h3-7H2,1-2H3

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:30536-44-8 SDS

30536-44-8Relevant articles and documents

2-AMINO-1,3,4-THIADIAZINE AND 2-AMINO-1,3,4-OXADIAZINE BASED ANTIFUNGAL AGENTS

-

Page/Page column 44, (2017/02/09)

The invention provides a compound which is a diazine of formula (I) or a tautomer thereof, or a pharmaceutically acceptable salt thereof, for use as an antifungal agent: (I) wherein X, N', C', A and E are as defined herein. The invention also provides a compound of Formula (I) as defined herein.

O-benzenedisulfonimide as a reusable brnsted acid catalyst for hetero-michael reactions

Barbero, Margherita,Cadamuro, Silvano,Dughera, Stefano

, p. 758 - 767 (2013/01/15)

The hetero-Michael reactions among various oxygen, sulfur, and nitrogen nucleophiles and ,-unsaturated compounds were carried out in the presence of catalytic amounts of o-benzenedisulfonimide as Brnsted acid organocatalyst. The reaction conditions were very mild, and the yields of target products were good. The catalyst was easily recovered and purified, ready to be used in further reactions. This ability grants economic and ecological advantages. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications to view the free supplemental file.

Heterobimetallic Pd-Sn catalysis: Michael addition reaction with C-, N-, O-, and S-nucleophiles and in situ diagnostics

Das, Debjit,Pratihar, Sanjay,Roy, Sujit

, p. 2430 - 2442 (2013/04/23)

An efficient Michael addition reaction of differently substituted enones with carbon, sulfur, oxygen, and nitrogen nucleophiles has been achieved by a new heterobimetallic "Pd-Sn" catalyst system. The nature of the catalytically relevant species and their

Acidic ionic liquid [NMP]H2PO4 as dual solvent-catalyst for synthesis of β-alkoxyketones by the oxa-Michael addition reactions

Guo, Hui,Li, Xia,Wang, Jun-Liang,Jin, Xiao-Han,Lin, Xian-Fu

experimental part, p. 8300 - 8303 (2010/11/05)

Acidic ionic liquid N-methyl-2-pyrrolidonium dihydrogen phosphate [NMP]H2PO4 was prepared and used as efficient catalyst and reaction medium to synthesize β-alkoxyketones by the oxa-Michael addition reactions for the first time. The

The ionic liquid ethyltri-n-butylphosphonium tosylate as solvent for the acid-catalysed hetero-Michael reaction

Karodia, Nazira,Liu, Xihan,Ludley, Petra,Pletsas, Dimitrios,Stevenson, Grace

, p. 11039 - 11043 (2007/10/03)

A new and convenient method for the acid-catalysed Michael addition reactions of alcohols, thiols and amines to methyl vinyl ketone has been developed using the ionic liquid ethyltri-n-butylphosphonium tosylate. The reaction conditions are mild and obviat

SUPERACID CATALYZED OXYGENATION OF ALIPHATIC ETHERS WITH OZONE

Yoneda, Norihiko,Kiuchi, Takashi,Fukuhara, Tsuyoshi,Suzuki, Akira,Olah, George A.

, p. 1617 - 1618 (2007/10/02)

Electrophilic insertion of protonated ozone into tertiary or secondary C-H bonds located at γ or farther away positions from the oxygen atom in aliphatic ethers was observed to produce oxoalkyl ethers in HF-SbF5 superacid media at -40 deg C.

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