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2,5-Piperazinedione,1-acetyl-4-methyl-3-methylene-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 182067-87-4 Structure
  • Basic information

    1. Product Name: 2,5-Piperazinedione,1-acetyl-4-methyl-3-methylene-(9CI)
    2. Synonyms: 2,5-Piperazinedione,1-acetyl-4-methyl-3-methylene-(9CI);1-(ACETYLOXY)-4-METHYL-3-METHYLIDENEPIPERAZINE-2,5-DIONE
    3. CAS NO:182067-87-4
    4. Molecular Formula: C8H10N2O3
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: PIPERIDINE
    8. Mol File: 182067-87-4.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: 2,5-Piperazinedione,1-acetyl-4-methyl-3-methylene-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,5-Piperazinedione,1-acetyl-4-methyl-3-methylene-(9CI)(182067-87-4)
    11. EPA Substance Registry System: 2,5-Piperazinedione,1-acetyl-4-methyl-3-methylene-(9CI)(182067-87-4)
  • 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: 182067-87-4(Hazardous Substances Data)

182067-87-4 Usage

General Description

2,5-Piperazinedione,1-acetyl-4-methyl-3-methylene-(9CI) is a chemical compound with the molecular formula C7H10N2O2. It is a derivative of piperazine and is commonly used as a building block in the synthesis of various chemical compounds and pharmaceuticals. 2,5-Piperazinedione,1-acetyl-4-methyl-3-methylene-(9CI) is known for its potential biological activities, including anti-inflammatory and antitumor properties. It is also used as an intermediate in the production of dyes, pigments, and other organic chemicals. Research on its applications and properties is ongoing, and it is considered to have potential value in various industrial and medical fields.

Check Digit Verification of cas no

The CAS Registry Mumber 182067-87-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,0,6 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 182067-87:
(8*1)+(7*8)+(6*2)+(5*0)+(4*6)+(3*7)+(2*8)+(1*7)=144
144 % 10 = 4
So 182067-87-4 is a valid CAS Registry Number.

182067-87-4SDS

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 (4-methyl-3-methylidene-2,5-dioxopiperazin-1-yl) acetate

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:182067-87-4 SDS

182067-87-4Downstream Products

182067-87-4Relevant articles and documents

Selectivity in radical reactions of alanylglycine anhydride derivatives

Chai, Christina L.L.,Hay, Darren B.,King, Alison R.

, p. 605 - 610 (2007/10/03)

Functionalization of N,N′-disubstituted alanylglycine anhydrides under radical conditions is described. The radical (7), generated (i) from reactions of N,N′-disubstituted alanylglycine anhydrides with N-bromosuccinimide, and (ii) from related bromo compounds by reaction with tributyltin deuteride, undergoes carbon-bromine and carbon-deuterium bond formation with moderate to high diastereoselectivities depending on the N-substituents present.

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