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21078-03-5

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21078-03-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21078-03-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,7 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21078-03:
(7*2)+(6*1)+(5*0)+(4*7)+(3*8)+(2*0)+(1*3)=75
75 % 10 = 5
So 21078-03-5 is a valid CAS Registry Number.

21078-03-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dimethyl-2-(prop-2-ynyloxy)benzene

1.2 Other means of identification

Product number -
Other names 1,3-dimethyl-2-prop-2-ynyloxybenzene

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:21078-03-5 SDS

21078-03-5Downstream Products

21078-03-5Relevant articles and documents

A short, vinyl radical cyclisation approach to (±))-2-pupukeanone

Srikrishna,Vijaykumar,Sharma

, p. 2003 - 2004 (1997)

Addition of tri-n-butyltin radical to a 5-(prop-2-ynyl)bicyclo [2.2.2]oct-2-ene followed by 5-exo-trig cyclisation of the resulting vinyl radical furnishes an isotwistane, providing a short route to the sesquiterpenes, pupukeananes 4 and 2.

Method for synthesizing mexiletine chloride

-

Paragraph 0031; 0032; 0033; 0034, (2019/03/15)

The invention discloses a method for synthesizing mexiletine chloride, wherein a reaction system takes 2,6-xylenol as a starting material to synthesize a corresponding target product. In the reaction,a transition metal gold complex and a ruthenium complex are used for catalysis, compared with the previous method for synthesizing mexiletine chloride, no alkali is added during a reaction process, no by-products are produced, the reaction atom economy is high, and the reaction conditions are mild. Therefore, the method has broad development prospects.

Formal total synthesis of 2-pupukeanone via radical mediated cyclisation of an enyne

Srikrishna,Vijaykumar,Sharma

, p. 766 - 770 (2007/10/03)

Diels-Alder reaction of the dienone 12, obtained by C-alkylation of sodium 2,6-dimethylphenoxide, with acrylonitrile and phenyl vinyl sulfones generate the enynes 14 and 17. Tributyltin radical addition to the terminal acetylene in 14 and 17 lead to the v

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