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CAS

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89064-05-1

7-Oxabicyclo[4.1.0]hept-2-ene, (1S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 89064-05-1 Structure

  • Basic information

    1. Product Name: 7-Oxabicyclo[4.1.0]hept-2-ene, (1S)-
    2. Synonyms:
    3. CAS NO:89064-05-1
    4. Molecular Formula: C6H8O
    5. Molecular Weight: 96.1289
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89064-05-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 7-Oxabicyclo[4.1.0]hept-2-ene, (1S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-Oxabicyclo[4.1.0]hept-2-ene, (1S)-(89064-05-1)
    11. EPA Substance Registry System: 7-Oxabicyclo[4.1.0]hept-2-ene, (1S)-(89064-05-1)

  • 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: 89064-05-1(Hazardous Substances Data)

89064-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89064-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,6 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 89064-05:
(7*8)+(6*9)+(5*0)+(4*6)+(3*4)+(2*0)+(1*5)=151
151 % 10 = 1
So 89064-05-1 is a valid CAS Registry Number.

89064-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4R)-3,4-epoxy-1-cyclohexene

1.2 Other means of identification

Product number -
Other names (1S,6R)-7-Oxa-bicyclo[4.1.0]hept-2-ene

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:89064-05-1 SDS

89064-05-1Relevant articles and documents

Enantioselective epoxidation of cyclic 1,3-dienes catalyzed by a sterically and electronically optimized (salen)Mn complex

Chang, Sukbok,Heid, Richard M.,Jacobsen, Eric N.

, p. 669 - 672 (2007/10/02)

Chiral (salen)Mn(III)Cl complexes catalyze epoxidation of cyclic 1,3-dienes with moderate-to-good enantioselectivity. A new catalyst (2), bearing sterically hindered and electron donating (OSi(iPr)3 (OTIPS) substituents, induces up to 12% higher selectivity than the previously-reported tert-butyl substituted analog 1.

STEREOSELECTIVE TOTAL SYNTHESIS OF (4S)-trans-β-ELEMENONE FROM (S)-2-CYCLOHEXEN-1-OL

Sato, Toshio,Gotoh, Yoshihiko,Watanabe, Makoto,Fujisawa, Tamotsu

, p. 1533 - 1536 (2007/10/02)

Stereoselective first total synthesis of (4S)-trans-β-elemenone was achieved from (S)-2-cyclohexen-1-ol, prepared easily by the asymmetric reduction of 2-cyclohexen-1-one with chiral hydride reagent.

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