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CAS

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77928-09-7

ethyl α-methylthio-4-allyloxy-3-chlorophenylacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 77928-09-7 Structure

  • Basic information

    1. Product Name: ethyl α-methylthio-4-allyloxy-3-chlorophenylacetate
    2. Synonyms: ethyl α-methylthio-4-allyloxy-3-chlorophenylacetate
    3. CAS NO:77928-09-7
    4. Molecular Formula:
    5. Molecular Weight: 300.806
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 77928-09-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ethyl α-methylthio-4-allyloxy-3-chlorophenylacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl α-methylthio-4-allyloxy-3-chlorophenylacetate(77928-09-7)
    11. EPA Substance Registry System: ethyl α-methylthio-4-allyloxy-3-chlorophenylacetate(77928-09-7)

  • 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: 77928-09-7(Hazardous Substances Data)

77928-09-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77928-09-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,9,2 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77928-09:
(7*7)+(6*7)+(5*9)+(4*2)+(3*8)+(2*0)+(1*9)=177
177 % 10 = 7
So 77928-09-7 is a valid CAS Registry Number.

77928-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-1-(1,3-dioxoisoindolin-2-yl)-3,3-dimethyltriaz-1-ene 2-oxide

1.2 Other means of identification

Product number -
Other names -

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:77928-09-7 SDS

77928-09-7Relevant articles and documents

Synthesis of Ethyl Arylacetates by Means of Friedel-Crafts Reaction of Aromatic Compounds with Ethyl α-Chloro-α-(methylthio)acetate

Tamura, Yasumitsu,Choi, Hong Dae,Shindo, Hirohisa,Ishibashi, Hiroyuki

, p. 915 - 921 (2007/10/02)

Friedel-Crafts reaction of aromatic compounds with ethyl α-chloro-α-(methylthio)acetate (1) gave ethyl α-(methylthio)arylacetates (2), which were readily converted into ethyl arylacetates (3) by reductive desulfurization with Raney nickel or zinc dust-acetic acid.The reactions were applied to the syntheses of ibufenac (5) and alclofenac (6), which are anti-inflammatory agents.

ELECTROPHILIC AROMATIC SUBSTITUTION BY PUMMERER REACTION OF α-SULFINYLACETATE

Tamura, Y.,Choi, H.-D.,Shindo, H.,Uenishi, J.,Ishibashi, H.

, p. 81 - 84 (2007/10/02)

Treatment of a mixture of aromatic compound and ethyl α-(methylsulfinyl)acetate (5) with p-toluenesulfonic acid under continuous removal of separated water brought about an intermolecular aromatic substitution to give ethyl α-(methylthio)arylacetate (6).S

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