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heptene-5 ol-1 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89794-36-5

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89794-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89794-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,9 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89794-36:
(7*8)+(6*9)+(5*7)+(4*9)+(3*4)+(2*3)+(1*6)=205
205 % 10 = 5
So 89794-36-5 is a valid CAS Registry Number.

89794-36-5SDS

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 5-Hepten-1-ol

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:89794-36-5 SDS

89794-36-5Relevant academic research and scientific papers

A novel hydrogen transfer hydroalumination of alkenes with triisobutylaluminum catalyzed by Pd and other late transition metal complexes

Gagneur, Sebastien,Makabe, Hidefumi,Negishi, Ei-Ichi

, p. 785 - 787 (2007/10/03)

Hydrogen transfer hydroalumination of terminal alkenes and dienes can be achieved with 1.1 equiv. of (i-Bu)3Al and catalytic amounts of Cl2Pd(PPh3)2 and other late transition metal complexes containing Co, Rh, Ni, and Pt at ambient temperature in high yields.

EVOLUTION THERMIQUE DE N-OXYDES DE DIMETHYLAMINO-5 ALCANOLS-1 SUBSTITUES EN 5. COMPETITION ENTRE REARRANGEMENTS DE COPE ET DE MEISENHEIMER

Barbry, Didier,Hasiak, Bruno,Augait, Jean-Michel,Couturier, Daniel

, p. 956 - 961 (2007/10/02)

The effect of the substituent R in the 5 position was studied in the decomposition of 1,5-aminoalcohol N-oxides: Meisenheimer rearrangements takes place when R is the vinyl group but is not observed with the phenyl substituent; elimination to alkenol only

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