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736127-53-0

CIS-(Z)-8-AMINO-CYCLOOCT-4-ENECARBOXYLIC ACID is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 736127-53-0 Structure

  • Basic information

    1. Product Name: CIS-(Z)-8-AMINO-CYCLOOCT-4-ENECARBOXYLIC ACID
    2. Synonyms: CIS-(Z)-8-AMINO-CYCLOOCT-4-ENECARBOXYLIC ACID
    3. CAS NO:736127-53-0
    4. Molecular Formula: C9H15NO2
    5. Molecular Weight: 169.22
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 736127-53-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 313.6°C at 760 mmHg
    3. Flash Point: 143.4°C
    4. Appearance: /
    5. Density: 1.091g/cm3
    6. Vapor Pressure: 0.000107mmHg at 25°C
    7. Refractive Index: 1.507
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: CIS-(Z)-8-AMINO-CYCLOOCT-4-ENECARBOXYLIC ACID(CAS DataBase Reference)
    11. NIST Chemistry Reference: CIS-(Z)-8-AMINO-CYCLOOCT-4-ENECARBOXYLIC ACID(736127-53-0)
    12. EPA Substance Registry System: CIS-(Z)-8-AMINO-CYCLOOCT-4-ENECARBOXYLIC ACID(736127-53-0)

  • 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: 736127-53-0(Hazardous Substances Data)

736127-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 736127-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,6,1,2 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 736127-53:
(8*7)+(7*3)+(6*6)+(5*1)+(4*2)+(3*7)+(2*5)+(1*3)=160
160 % 10 = 0
So 736127-53-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H15NO2/c10-8-6-4-2-1-3-5-7(8)9(11)12/h1-2,7-8H,3-6,10H2,(H,11,12)/b2-1-/t7-,8+/m1/s1

736127-53-0SDS

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 CIS-(Z)-8-AMINO-CYCLOOCT-4-ENECARBOXYLIC ACID

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:736127-53-0 SDS

736127-53-0Upstream product

736127-53-0Downstream Products

736127-53-0Relevant articles and documents

Helical folding of α/β-peptides containing β-amino acids with an eight-membered ring constraint

Lee, Woohyung,Kwon, Sunmi,Kang, Philjae,Guzei, Ilia A.,Choi, Soo Hyuk

supporting information, p. 2641 - 2644 (2014/05/06)

αβα-Tripeptide that contains a cyclic β-amino acid with an eight-membered ring, a cis-2-aminocyclooct-5-enecarboxylic acid (cis-ACOE) or a cis-2-aminocyclooctanecarboxylic acid (cis-ACOC) displayed an 11/9-helical turn in the crystal state. The related α/β-peptide oligomers were shown to adopt 11/9-helical conformations in solution. This journal is the Partner Organisations 2014.

Synthesis of mono- and dihydroxy-substituted 2-aminocyclooctanecarboxylic acid enantiomers

Palko, Marta,Benedek, Gabriella,Forro, Enik,Weber, Edit,Haenninen, Mikko,Sillanpaeae, Reijo,Fueloep, Ferenc

experimental part, p. 957 - 961 (2010/08/06)

(1R,2S,6R)-2-Amino-6-hydroxycyclooctanecarboxylic acid (-)-10 was synthesized from (1R,2S)-2-aminocyclooct-5-enecarboxylic acid (+)-2 via an iodolactone intermediate, while (1R,2S,3R,4S)-2-amino-5,6- dihydroxycyclooctanecarboxylic acid (-)-12 was prepared

Advanced procedure for the enzymatic ring opening of unsaturated alicyclic β-lactams

Forro, Eniko,Fueloep, Ferenc

, p. 2875 - 2880 (2007/10/03)

Enantiopure β-amino acids 1a-4a and β-lactams 1b-4b were prepared simultaneously through the lipolase-catalysed enantioselective ring opening of unsaturated racemic β-lactams (±)-1-(±)-4. High enantioselectivities (E>200) were observed when the reactions

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