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60858-07-3

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60858-07-3 Usage

Furan derivative

Yes, with a hexenyl side chain and a methyl group

Natural sources

Coffee, cocoa, roasted peanuts

Aroma and flavor

Sweet, nutty scent, contributes to the characteristic aroma and flavor of the natural sources

Usage

Flavor and fragrance industry, used as a component in various products (perfumes, soaps, and other scented items)

Potential properties

Antioxidant, antimicrobial, useful in food and pharmaceutical industries

Check Digit Verification of cas no

The CAS Registry Mumber 60858-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,5 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60858-07:
(7*6)+(6*0)+(5*8)+(4*5)+(3*8)+(2*0)+(1*7)=133
133 % 10 = 3
So 60858-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O/c1-3-4-5-6-7-11-9-8-10(2)12-11/h4-5,8-9H,3,6-7H2,1-2H3

60858-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-Hexenyl)-5-Methylfuran

1.2 Other means of identification

Product number -
Other names 2-(Hex-3-Enyl)-5-Methyl-Furan

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:60858-07-3 SDS

60858-07-3Downstream Products

60858-07-3Relevant articles and documents

Nickel-Catalyzed Migratory Hydrocyanation of Internal Alkenes: Unexpected Diastereomeric-Ligand-Controlled Regiodivergence

Gao, Jihui,Jiao, Mingdong,Ni, Jie,Yu, Rongrong,Cheng, Gui-Juan,Fang, Xianjie

supporting information, p. 1883 - 1890 (2020/12/01)

A regiodivergent nickel-catalyzed hydrocyanation of a broad range of internal alkenes involving a chain-walking process is reported. When appropriate diastereomeric biaryl diphosphite ligands are applied, the same starting materials can be converted to either linear or branched nitriles with good yields and high regioselectivities. DFT calculations suggested that the catalyst architecture determines the regioselectivity by modulating electronic and steric interactions. In addition, moderate enantioselectivities were observed when branched nitriles were produced.

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