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2-Hexen-1-ol, 5-methyl, (E)-, also known as leaf alcohol, is a naturally occurring organic compound with the chemical formula C6H12O. It is a colorless liquid with a strong, green, leafy odor, and is an important component in the fragrance industry. 2-Hexen-1-ol, 5-methyl-, (E)- is a primary constituent of green leaf volatiles, which are responsible for the characteristic smell of freshly cut grass and green leaves. It is widely used in perfumery to create natural, fresh, and green scents, and can also be found in various essential oils, such as lavender, rosemary, and citrus. The (E)- configuration in its name indicates the geometric isomerism of the double bond present in the molecule, which plays a role in its distinct odor and properties.

1589-35-1

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1589-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1589-35-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,8 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1589-35:
(6*1)+(5*5)+(4*8)+(3*9)+(2*3)+(1*5)=101
101 % 10 = 1
So 1589-35-1 is a valid CAS Registry Number.

1589-35-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-5-methylhex-2-en-1-ol

1.2 Other means of identification

Product number -
Other names (E)-5-methylhex-2-en-1-ol

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:1589-35-1 SDS

1589-35-1Relevant academic research and scientific papers

NICKEL(II)-CATALYZED ALKYLATION OF 2-METHYL-1,3-DIOXEP-4-ENE BY GRIGNARD REAGENTS: AN EFFICIENT AND SELECTIVE ROUTE TO ALLYLIC ALCOHOLS

Menicagli, Rita,Malanga, Corrado,Finato, Barbara,Lardicci, Luciano

, p. 69 - 70 (2007/10/02)

Allylic alcohols are formed, in good yields, through the regiocontrolled Cl2Nidppe-catalyzed alkylation of 2-methyl-1,3-dioxep-4-ene by Grignard reagents .Highly pure Z alcohols arise when secondary and tertiary aliphatic Grignards are used.

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