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19275-29-7

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19275-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19275-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,7 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 19275-29:
(7*1)+(6*9)+(5*2)+(4*7)+(3*5)+(2*2)+(1*9)=127
127 % 10 = 7
So 19275-29-7 is a valid CAS Registry Number.

19275-29-7SDS

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-ethynyl-5-nitrofuran

1.2 Other means of identification

Product number -
Other names 5-nitro-2-furylacetylene

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:19275-29-7 SDS

19275-29-7Downstream Products

19275-29-7Relevant articles and documents

An efficient method for the production of terminal alkynes from 1,1-dibromo-1-alkenes and its application in the total synthesis of natural product dihydroxerulin

Liu, Shihui,Chen, Xiaobei,Hu, Yanwei,Yuan, Laiqi,Chen, Shaohua,Wu, Ping,Wang, Wei,Zhang, Shilei,Zhang, Wei

, p. 553 - 560 (2015/03/05)

An efficient method of preparing various terminal alkynes from 1,1-dibromo-1-alkenes by using TBAF (tetra-n-butylammonium fluoride) as a base and triphenylphosphane as a reductant was developed. This method is strong base and low/high temperatures free, and can tolerate a broad range of substrates. These advantages were well demonstrated by the application of this method to the total synthesis of polyene natural product dihydroxerulin.

5-Nitro-2-furylvinylation of Secondary and Tertiary Amines

Vegh, Daniel,Kovac, Jaroslav,Dandarova, Miloslava,Ivanco, Lubor

, p. 155 - 162 (2007/10/02)

Reaction of 12 secondary amines and trimethylamine with (Z) and (E)-5-nitro-2-furylvinylbromide (I) was studied.Whereas the enamine II, obtained from secondary amines, have the E configuration, the quaternisation of trimethyamine affords stereospecifically the corresponding (Z) or (E) vinylammonium salts III.

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