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709-12-6

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709-12-6 Usage

Presence

Household products, fragrances, and essential oils

Physical state

Colorless liquid at room temperature

Usage

Flavoring agent in food products and beverages

Odor

Sweet, woody, and slightly spicy

Application

Ingredient in perfumes and air fresheners

Therapeutic benefits

Anti-inflammatory and pain-relieving properties

Caution

Consult a healthcare professional before using for medicinal purposes

Check Digit Verification of cas no

The CAS Registry Mumber 709-12-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 709-12:
(5*7)+(4*0)+(3*9)+(2*1)+(1*2)=66
66 % 10 = 6
So 709-12-6 is a valid CAS Registry Number.

709-12-6SDS

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 1-(cyclopenten-1-yl)-4-methoxybenzene

1.2 Other means of identification

Product number -
Other names F0701-0013

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:709-12-6 SDS

709-12-6Relevant articles and documents

Nickel-catalyzed Heck reaction of cycloalkenes using aryl sulfonates and pivalates

Zhou, Jianrong Steve,Huang, Xiaolei,Teng, Shenghan,Chi, Yonggui Robin

supporting information, p. 3933 - 3936 (2021/04/26)

Nickel-catalyzed Heck reaction of cycloalkenes delivers unusual conjugated arylated isomers. Nickel(0) catalysts ligated by chelating dialkylphosphines effectively activate not only aryl triflates as electrophiles, but also less reactive aryl mesylates, t

Enantioselective Copper Catalyzed Alkyne-Azide Cycloaddition by Dynamic Kinetic Resolution

Liu, En-Chih,Topczewski, Joseph J.

, p. 5135 - 5138 (2019/03/29)

The copper(I) catalyzed alkyne-azide cycloaddition (CuAAC), a click reaction, is one of the most powerful catalytic reactions developed during the last two decades. Conducting CuAAC enantioselectively would add a third dimension to this reaction and would

Cyclopentene Annulations of Alkene Radical Cations with Vinyl Diazo Species Using Photocatalysis

Sarabia, Francisco J.,Li, Qiankun,Ferreira, Eric M.

supporting information, p. 11015 - 11019 (2018/07/30)

A direct (3+2) cycloaddition between alkenes and vinyl diazo reagents using either Cr or Ru photocatalysis is described. The intermediacy of a radical cation species enables a nucleophilic interception by vinyl diazo compounds, a departure from their trad

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