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CAS

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138457-95-1

Cyclopropanecarboxylic acid, 1-amino-2-ethyl-, methyl ester, (1S-cis)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Cyclopropanecarboxylic acid, 1-amino-2-ethyl-, methyl ester, (1S-cis)- (9CI)

    Cas No: 138457-95-1

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  • 138457-95-1 Structure

  • Basic information

    1. Product Name: Cyclopropanecarboxylic acid, 1-amino-2-ethyl-, methyl ester, (1S-cis)- (9CI)
    2. Synonyms: Cyclopropanecarboxylic acid, 1-amino-2-ethyl-, methyl ester, (1S-cis)- (9CI)
    3. CAS NO:138457-95-1
    4. Molecular Formula: C7H13NO2
    5. Molecular Weight: 143.18362
    6. EINECS: N/A
    7. Product Categories: AMINOACID;CARBOXYLICESTER
    8. Mol File: 138457-95-1.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: Cyclopropanecarboxylic acid, 1-amino-2-ethyl-, methyl ester, (1S-cis)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclopropanecarboxylic acid, 1-amino-2-ethyl-, methyl ester, (1S-cis)- (9CI)(138457-95-1)
    11. EPA Substance Registry System: Cyclopropanecarboxylic acid, 1-amino-2-ethyl-, methyl ester, (1S-cis)- (9CI)(138457-95-1)

  • 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: 138457-95-1(Hazardous Substances Data)

138457-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138457-95-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,5 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138457-95:
(8*1)+(7*3)+(6*8)+(5*4)+(4*5)+(3*7)+(2*9)+(1*5)=161
161 % 10 = 1
So 138457-95-1 is a valid CAS Registry Number.

138457-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl (1S,2R)-(-)-1-Amino-2-ethyl-1-cyclopropanecarboxylate

1.2 Other means of identification

Product number -
Other names (1S,2R)-1-Amino-2-ethyl-cyclopropanecarboxylic acid methyl 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:138457-95-1 SDS

138457-95-1Relevant articles and documents

Asymmetric Synthesis via Heterocyclic Intermediates, XLVII. Asymmetric Synthesis of (+)-(1R,2S)-allo-Coronamic Acid

Groth, Ulrich,Halfbrodt, Wolfgang,Schoellkopf, Ulrich

, p. 351 - 356 (2007/10/02)

allo-Coronamic acid (1) was synthesized in five steps enantiomerically and diastereomerically virtually pure by starting from the bislactim ethers of cyclo(-L-Val-Gly-) (3a) or cyclo(-L-tert-Leu-Gly-) (3b) in an overall yield of 31percent.The key step of this synthesis is the intramolecular alkylation of the lithium azaenolate derived from the allylic chloride 4. Key Words: Amino acids / Cyclopropanes / Cyclopropanation, diastereoselective / Bislactim ether method

A CONVENIENT SYNTHESIS OF REGIO-SPECIFICALLY 2-ALKYLATED-3-DEUTERIATED-1-AMINOCYCLOPROPANE-1-CARBOXYLIC ACIDS

Baldwin, Jack E.,Adlington, Robert M.,Rawlings, Bernard J.

, p. 481 - 484 (2007/10/02)

A simple procedure for the large scale preparations of regio-specifically 2-alkylated-3-deuteriated-1-aminocyclopropane-1-carboxylic acids from 1-deuterio-1,2-dibromoalkanes is described.

SYNTHESIS OF 1-AZIDOCYCLOPROPANECARBOXYLATES FROM 2-AZIDO-2-ALKENOATES

Hiyama, Tamejiro,Kai, Mariko

, p. 2103 - 2104 (2007/10/02)

Addition of diazomethane to 2-azido-2-alkenoates followed by pyrolysis of the resulting pyrazoline derivatives affords the title compounds.

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