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Benzene, 1-[(1,1-dimethyl-2-propynyl)oxy]-4-iodo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129180-58-1

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129180-58-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129180-58-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,1,8 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 129180-58:
(8*1)+(7*2)+(6*9)+(5*1)+(4*8)+(3*0)+(2*5)+(1*8)=131
131 % 10 = 1
So 129180-58-1 is a valid CAS Registry Number.

129180-58-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-iodo-4-(2-methylbut-3-yn-2-yloxy)benzene

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:129180-58-1 SDS

129180-58-1Downstream Products

129180-58-1Relevant academic research and scientific papers

Improved Synthesis of Aryl 1,1-Dimethylpropargyl Ethers

Godfrey, Jollie D.,Mueller, Richard H.,Sedergran, Thomas C.,Soundarajan, Nachimuthu,Colandrea, Vincent J.

, p. 6405 - 6408 (1994)

An efficient, general, and practical synthesis of aryl 1,1-dimethylpropargyl ethers has been developed.

Copper-catalyzed intramolecular carbotrifluoromethylation of alkynes for the construction of trifluoromethylated heterocycles

Wang, Yanan,Jiang, Min,Liu, Jin-Tao

supporting information, p. 15315 - 15319 (2016/02/18)

A mild and efficient copper-catalyzed intramolecular carbotrifluoromethylation of alkynes has been achieved in the presence of Togni reagent as trifluoromethylating reagent. The reaction tolerates a range of substrates to give a group of trifluoromethylated heterocycles with high selectivities. A plausible mechanism was proposed on the basis of experimental results. And the Togni award goes to Copper-catalyzed intramolecular carbotrifluoromethylation of alkynes is carried out with a Togni reagent as the trifluoromethylating reagent (see scheme). Various trifluoromethylated heterocycles are synthesized in moderate to good yields. Moreover, a range of common functional groups is tolerated under the reaction conditions.

Phosphinic ester substituted benzopyran derivatives

-

, (2008/06/13)

STR1 and pharmaceutically acceptable salts thereof wherein Y is a single bond, --CH 2 --, --C(O)--, --S-- or --N(R 11)--; and R 1 to R 6 are as defined herein. These compounds have potassium channel activating activity and are useful, therefore for example, as cardiovascular agents.

Copper(I) iodide: A catalyst for the improved synthesis of aryl propargyl ethers

Bell,Davies,Geen,Mann

, p. 707 - 712 (2007/10/02)

Copper(I) iodide catalyses the reaction between phenols and dialkylpropargyl chlorides to give aryl 1,1-dialkylpropargyl ethers 5 a-k and 7a-e in good yields and purity. These ethers are important as precursors to the 2H-1-benzopyrans 8a-l and 9a-e.

Benzopyran derivatives and antihypertensive use thereof

-

, (2008/06/13)

Disclosed herein are novel benzopyrans having pharmacological activity, to a process for preparing them, to pharmaceutical compositions containing them, and to their use in the treatment of hypertension.

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