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111508-33-9

Diazenedicarboxylic acid, ethyl phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 111508-33-9 Structure

  • Basic information

    1. Product Name: Diazenedicarboxylic acid, ethyl phenylmethyl ester
    2. Synonyms:
    3. CAS NO:111508-33-9
    4. Molecular Formula: C11H12N2O4
    5. Molecular Weight: 236.227
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 111508-33-9.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: Diazenedicarboxylic acid, ethyl phenylmethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Diazenedicarboxylic acid, ethyl phenylmethyl ester(111508-33-9)
    11. EPA Substance Registry System: Diazenedicarboxylic acid, ethyl phenylmethyl ester(111508-33-9)

  • 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: 111508-33-9(Hazardous Substances Data)

111508-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111508-33-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,5,0 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 111508-33:
(8*1)+(7*1)+(6*1)+(5*5)+(4*0)+(3*8)+(2*3)+(1*3)=79
79 % 10 = 9
So 111508-33-9 is a valid CAS Registry Number.

111508-33-9SDS

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 benzyl ethyl diazene-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names 1,2-Diazenedicarboxylic Acid 1-Ethyl 2-(phenylmethyl) Ester

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:111508-33-9 SDS

111508-33-9Relevant articles and documents

FIVE-MEMBERED HETEROCYCLIC DERIVATIVE

-

Page/Page column 34, (2010/11/08)

The present invention relates to a compound represented by formula (I): a salt of the compound, or a solvate of the compound or the salt; a drug containing any of the compounds, the salts, and the solvates; a preventive and/or therapeutic agent for an ischemic disease containing any of the compounds, the salts, and the solvates; and a platelet coagulation inhibitor containing any of the compounds, the salts, and the solvates. The compound of the present invention is useful as a strong platelet coagulation inhibitor without inhibiting COX-1 or COX-2.

Synthesis of 1,2-Diazetidinones (Aza-β-lactams) by Photochemical Ring Contraction

Lawton, Geoffrey,Moody, Christopher J.,Pearson, Christopher J.

, p. 877 - 884 (2007/10/02)

Irradiation of 4-diazopyrazolidine-3,5-diones (11) in the presence of alcohols, diethylamine, or water gives 1,2-diazetidinones (12) formed by photochemical Wolff rearrangement with ring contraction followed by reaction of the resulting ketene with the nucleophile.In the case of the bicyclic diazo compound (11d) a fragmentation reaction competes with ring contraction.The aza-β-lactams (12) show the expected high frequency carbonyl stretch in their i.r. spectra.The acid (12e) readily decarboxylates to give the 4-unsubstituted 1,2-dibenzyldiazetidinone (28), the four-membered ring of which is cleaved by alkaline hydrolysis, lithium aluminium hydride or diborane to give (29), (30), and (31), respectively (Scheme 9).Attempts to modify the carboxy substituent of (12e) into an acylamino group were unsuccessful.

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