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Pyrrolo[1,2-a]pyrazine-1,4-dione, hexahydro-3-hydroxy-3-methyl-, (8aS)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Pyrrolo[1,2-a]pyrazine-1,4-dione, hexahydro-3-hydroxy-3-methyl-, (8aS)- (9CI)

    Cas No: 302790-90-5

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  • Pyrrolo[1,2-a]pyrazine-1,4-dione, hexahydro-3-hydroxy-3-methyl-, (8aS)- (9CI)

    Cas No: 302790-90-5

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  • 302790-90-5 Structure
  • Basic information

    1. Product Name: Pyrrolo[1,2-a]pyrazine-1,4-dione, hexahydro-3-hydroxy-3-methyl-, (8aS)- (9CI)
    2. Synonyms: Pyrrolo[1,2-a]pyrazine-1,4-dione, hexahydro-3-hydroxy-3-methyl-, (8aS)- (9CI);(8AS)-3-HYDROXY-3-METHYLHEXAHYDROPYRROLO[1,2-A]PYRAZINE-1,4-DIONE
    3. CAS NO:302790-90-5
    4. Molecular Formula: C8H12N2O3
    5. Molecular Weight: 184.19248
    6. EINECS: N/A
    7. Product Categories: PIPERIDINE
    8. Mol File: 302790-90-5.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: Pyrrolo[1,2-a]pyrazine-1,4-dione, hexahydro-3-hydroxy-3-methyl-, (8aS)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pyrrolo[1,2-a]pyrazine-1,4-dione, hexahydro-3-hydroxy-3-methyl-, (8aS)- (9CI)(302790-90-5)
    11. EPA Substance Registry System: Pyrrolo[1,2-a]pyrazine-1,4-dione, hexahydro-3-hydroxy-3-methyl-, (8aS)- (9CI)(302790-90-5)
  • 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: 302790-90-5(Hazardous Substances Data)

302790-90-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 302790-90-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,7,9 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 302790-90:
(8*3)+(7*0)+(6*2)+(5*7)+(4*9)+(3*0)+(2*9)+(1*0)=125
125 % 10 = 5
So 302790-90-5 is a valid CAS Registry Number.

302790-90-5SDS

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 (8aS)-3-Hydroxy-3-methylhexahydropyrrolo[1,2-a]pyrazine-1,4-dione

1.2 Other means of identification

Product number -
Other names 6-Hepten-2-one,3-hydroxy-3-methyl

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:302790-90-5 SDS

302790-90-5Downstream Products

302790-90-5Relevant articles and documents

A synthetic model for the [4+2] cycloaddition in the biosynthesis of the brevianamides, paraherquamides, and related compounds

Sanz-Cervera, Juan F.,Williams, Robert M.,Alberto Marco,María López-Sánchez, José,González, Florenci,Eugenia Martínez, María,Sancenón, Félix

, p. 6345 - 6358 (2000)

The reactivity of model systems for the proposed [4+2] cycloaddition in the biosynthesis of the brevianamides, paraherquamides, and marcfortines is explored. The model for the intermolecular reaction reveals that the cycloaddition takes place under mild conditions only if activated, very reactive dienophiles are used. When relatively unreactive dienophiles such as cyclopentene and cyclohexene are used, harsh reaction conditions and/or a Lewis acid catalyst are necessary for the reaction. In contrast, the model for the intramolecular reaction demonstrates that the cycloaddition takes place within a few hours at room temperature, even in the absence of a Lewis acid catalyst. Conclusions drawn from these results are discussed in relation to the biosynthesis of the aforementioned metabolites. (C) 2000 Elsevier Science Ltd.

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