Welcome to LookChem.com Sign In|Join Free

CAS

  • or
1-Piperidineacetic acid, Methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58583-90-7 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 58583-90-7 Structure
  • Basic information

    1. Product Name: 1-Piperidineacetic acid, Methyl ester
    2. Synonyms: 1-Piperidineacetic acid, Methyl ester;methyl piperidin-1-ylacetate
    3. CAS NO:58583-90-7
    4. Molecular Formula: C8H15NO2
    5. Molecular Weight: 157.2102
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 58583-90-7.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-Piperidineacetic acid, Methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Piperidineacetic acid, Methyl ester(58583-90-7)
    11. EPA Substance Registry System: 1-Piperidineacetic acid, Methyl ester(58583-90-7)
  • 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: 58583-90-7(Hazardous Substances Data)

58583-90-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58583-90-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,8 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58583-90:
(7*5)+(6*8)+(5*5)+(4*8)+(3*3)+(2*9)+(1*0)=167
167 % 10 = 7
So 58583-90-7 is a valid CAS Registry Number.

58583-90-7SDS

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 methyl 2-piperidin-1-ylacetate

1.2 Other means of identification

Product number -
Other names methyl 2-piperidylacetate

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:58583-90-7 SDS

58583-90-7Relevant articles and documents

DICATION COMPOUND, PREPARATION METHOD THEREOF AND USE THEREOF

-

Paragraph 0041-0042, (2021/07/17)

A dication compound represented by formula (I), stereoisomers having the structure of formula (I) or a mixture of the stereoisomers, a pharmaceutically acceptable salt, a solvate, or a eutectic crystal, and a composition thereof, and use of a composition, are capable of producing neuromuscular junction retardation, formed of same with a pharmaceutically acceptable carrier in the field of preparation of a medicament for muscular flaccidity.

Cyano-containing biquaternary ammonium compound as well as preparation method and application thereof

-

Paragraph 0098-0100, (2021/07/10)

The invention relates to a cyano-containing biquaternary ammonium compound as well as a preparation method and application thereof, and particularly discloses a biquaternary ammonium compound as shown in a formula (I), or a crystal form, a solvate, a stereoisomer, an isotope substitute or a salt thereof. The biquaternary ammonium compound does not contain nitro, so that the potential safety hazard of nitro-containing compounds is effectively avoided; meanwhile, the biquaternary ammonium compound is low in single-time medication dosage and quick in effect taking, can provide a thorough muscle relaxation effect for 2-10 minutes, can realize a super-short-acting non-depolarization muscle relaxation effect only by depending on metabolism of an organism, and quickly and automatically fades after playing the super-short-acting muscle relaxation effect. Therefore, the biquaternary ammonium compound, or the crystal form thereof, or the solvate thereof, or the stereoisomer thereof, or the isotope substitute thereof, or the salt thereof provided by the invention has a very good application prospect in preparation of skeletal muscle relaxation drugs with low dosage, quick effect, quick recovery and small toxic and side effects.

A formal method for the de-N,N-dialkylation of Sommelet-Hauser rearrangement products

Tayama, Eiji,Sato, Ryota,Takedachi, Keisuke,Iwamoto, Hajime,Hasegawa, Eietsu

experimental part, p. 4710 - 4718 (2012/07/28)

Selective amine de-alkylation enables the conversion of Sommelet-Hauser rearrangement products into 2-aryl-2-bromoacetic acid derivatives. These compounds are valuable synthetic intermediates in the synthesis of α-aryl-α-amino or α-aryl-β-amino acid deriv

POSITIVE RESIST COMPOSITION AND PATTERNING PROCESS

-

, (2010/04/23)

A positive resist composition comprises (A) a resin component which becomes soluble in an alkaline developer under the action of an acid and (B) an acid generator. The resin (A) is a polymer comprising recurring units containing a non-leaving hydroxyl group represented by formula (1) wherein R1 is H, methyl or trifluoromethyl, X is a single bond or methylene, m is 1 or 2, and the hydroxyl group attaches to a secondary carbon atom. The composition is improved in resolution when processed by lithography.

Reaction of methyl diazoacetate with amines catalyzed by Ru 2(OAc)4Cl

Maidanova,Bakeeva,Sultanova,Biglova,Dokichev

experimental part, p. 1461 - 1465 (2011/03/17)

Reactions of primary and secondary amines with methyl diazoacetate in the presence of Ru2(OAc)4Cl gave the corresponding N-substituted glycine methyl esters in almost quantitative yield. Catalytic decomposition of methyl diazoacetate

Novel tertiary (meth)acrylates having lactone structure, polymers, resist compositions and patterning process

-

, (2008/06/13)

Novel tertiary (meth)acrylate compounds having a lactone structure are polymerizable into polymers having improved transparency, especially at the exposure wavelength of an excimer laser and dry etching resistance. Resist compositions comprising the polymers are sensitive to high-energy radiation, have a high resolution, and lend themselves to micropatterning with electron beams or deep-UV rays.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 58583-90-7