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109071-38-7

1-[(acetyloxy)Methyl]-2-Pyrrolidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 109071-38-7 Structure

  • Basic information

    1. Product Name: 1-[(acetyloxy)Methyl]-2-Pyrrolidinone
    2. Synonyms: 1-[(acetyloxy)Methyl]-2-Pyrrolidinone
    3. CAS NO:109071-38-7
    4. Molecular Formula: C7H11NO3
    5. Molecular Weight: 157.16714
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 109071-38-7.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: 1-[(acetyloxy)Methyl]-2-Pyrrolidinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-[(acetyloxy)Methyl]-2-Pyrrolidinone(109071-38-7)
    11. EPA Substance Registry System: 1-[(acetyloxy)Methyl]-2-Pyrrolidinone(109071-38-7)

  • 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: 109071-38-7(Hazardous Substances Data)

109071-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109071-38-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,0,7 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 109071-38:
(8*1)+(7*0)+(6*9)+(5*0)+(4*7)+(3*1)+(2*3)+(1*8)=107
107 % 10 = 7
So 109071-38-7 is a valid CAS Registry Number.

109071-38-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-oxopyrrolidin-1-yl)methyl acetate

1.2 Other means of identification

Product number -
Other names N-(Acetoxymethyl)-2-pyrrolidon

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:109071-38-7 SDS

109071-38-7Downstream Products

109071-38-7Relevant articles and documents

Pyroacm Resin: An Acetamidomethyl Derived Resin for Solid Phase Synthesis of Peptides through Side Chain Anchoring of C-Terminal Cysteine Residues

Juvekar, Vinayak,Gong, Young Dae

, p. 836 - 839 (2016)

The design, synthesis and utilization of an efficient acetamidomethyl derived resin for the peptide synthesis is presented using established Fmoc and Boc protocols via side chain anchoring. Cleavage of the target peptide from the resin is performed using carboxymethylsulfenyl chloride under mild conditions which gave in situ thiol-sulfenyl protection of the cysteine residues. The utility of the resin is successfully demonstrated through applications to the syntheses of model peptides and natural products Riparin 1.1 and Riparin 1.2. (Chemical Equation Presented).

HALOSILANES IN THE SYNTHESIS OF N-(HALOMETHYL) DERIVATIVES OF LACTAMS, N-METHYLCARBOXAMIDES, AND IMIDES

Orlova, N.A.,Shipov, A.G.,Savost'yanova, I.A.,Baukov, Yu.I.

, p. 1875 - 1881 (2007/10/02)

Methods are proposed for the synthesis of N-(halomethyl) derivatives of lactams, N-methylcarboxamides, and imides with the use of the paraform-chlorotrimethylsilane system and the replacement of the trimethylsiloxy group by halogen and of halogen by halogen by the action of halotrimethylsilanes or acetyl bromide.The reactions of N-(chloromethyl)lactams with carboxylic anhydrides lead to N-(acyloxymethyl)lactams.

Photoreactions of Succinimides with an N-Acyl Group in the Side Chain. Synthesis and Stereochemistry of Tricyclic Pyrrolopyrazine Ring Systems

Takechi, Haruko,Tateuchi, Sumiko,Machida, Minoru,Nishibata, Yoshihiko,Aoe, Keiichi,et al.

, p. 3142 - 3152 (2007/10/02)

Photocyclization of succinimides with an N-acyl group in the side chain gave bi- and tricyclic pyrrolopyrazines, some of which were converted to tricyclic amines by reduction.The stereochemistry of pyrrolopyrazine derivatives is discussed on the basis of the results of X-ray analysis and carbon-13 nuclear magnetic resonance spectroscopy.Keywords - succinimide; photocyclization; pyrrolo-pyrazine; hydrogen abstraction; X-ray analysis; 13C-NMR spectrum; tricyclic diamine

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