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o-hexynylbenzoic acid chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

205250-14-2

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205250-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 205250-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,2,5 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 205250-14:
(8*2)+(7*0)+(6*5)+(5*2)+(4*5)+(3*0)+(2*1)+(1*4)=82
82 % 10 = 2
So 205250-14-2 is a valid CAS Registry Number.

205250-14-2Relevant academic research and scientific papers

PhI(OCOCF3)2-Mediated Cyclization of o -(1-Alkynyl)benzamides: Metal-Free Synthesis of 3-Hydroxy-2,3-dihydroisoquinoline-1,4-dione

Yang, Chao,Zhang, Xiang,Zhang-Negrerie, Daisy,Du, Yunfei,Zhao, Kang

, p. 5320 - 5328 (2015/05/27)

The synthesis of an undocumented skeleton of 3-hydroxy-2,3-dihydroisoquinoline-1,4-diones has been discovered and reported. The reaction consists of an intramolecular cyclization of o-(1-alkynyl)benzamides in MeCN/H2O, mediated by metal-free, h

Reaction of 2-alkynylbenzoyl cyanides with carboxylic acids producing functionalized indenones

Shimizu, Hiroshi,Murakami, Masahiro

experimental part, p. 1817 - 1820 (2009/04/16)

2-Alkynylbenzoyl cyanides react with carboxylic acids via a cyclic allene intermediate to produce 2-acylamino-3-acylindenones in good yield. The high reactivity of the 2-acylamino moiety of the product for a substitution reaction can be utilized for the s

An Efficient Stereospecific Preparation of (Z)-3-Methylidene-selenophthalides and (Z)-3-Methylidenetellurophthalides [1]

Sashida, Haruki,Kawamukai, Atsushi

, p. 165 - 167 (2007/10/03)

(Z)-3-Methylideneselenophthalides 5A and (Z)-3-methylidenetellurophthalides 5B were easily prepared by the regioselective and stereoselective reaction of 2-ethynylbenzoyl chlorides 3 with sodium hydroselenide and sodium hydrotelluride in good yields, resp

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