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CAS

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38477-05-3

2,2-Diethyl-3-butenoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 38477-05-3 Structure

  • Basic information

    1. Product Name: 2,2-Diethyl-3-butenoic acid
    2. Synonyms: 2,2-Diethyl-3-butenoic acid
    3. CAS NO:38477-05-3
    4. Molecular Formula: C8H14O2
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 38477-05-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,2-Diethyl-3-butenoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-Diethyl-3-butenoic acid(38477-05-3)
    11. EPA Substance Registry System: 2,2-Diethyl-3-butenoic acid(38477-05-3)

  • 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: 38477-05-3(Hazardous Substances Data)

38477-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38477-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,7 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38477-05:
(7*3)+(6*8)+(5*4)+(4*7)+(3*7)+(2*0)+(1*5)=143
143 % 10 = 3
So 38477-05-3 is a valid CAS Registry Number.

38477-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-diethylbut-3-enoic acid

1.2 Other means of identification

Product number -
Other names 2,2-Diethylbut-3-enoesaeure

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:38477-05-3 SDS

38477-05-3Relevant articles and documents

Regioselective synthesis of 3,3-diethyl-4-(methylene)-1-quinol-2-ones by an intramolecular microwave assisted heck reaction

Smalley Jr., Terrence L.,Mills, Wendy Y.

, p. 327 - 331 (2007/10/03)

A protocol for the intramolecular Heck cyclization to afford 3,3-diethyl-4-(methylene)-1-quinol-2-ones is described. We observed that the use of microwave irradiation increased the efficiency of the reaction. Several examples are presented which show the

Regioselective Synthesis of β,γ-Unsaturated Acids by the Electrochemical Carboxylation of Allylic Bromides Using a Reactive-metal Anode

Tokuda, Masao,Kabuki, Takashi,Katoh, Yoshitaka,Suginome, Hiroshi

, p. 3345 - 3348 (2007/10/02)

Electrolysis of γ-mono and disubstituted allylic bromides in the presence of atmospheric pressure of carbon dioxide using a platinum cathode and a magnesium anode gave regioselectively the corresponding γ-mono and disubstituted β,γ-unsaturated carboxylic acids in 34-71percent yields.

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