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Benzamide, N-chloro-N-methyl-, also known as N-chloro-N-methylbenzamide or CMBA, is an organic compound with the chemical formula C8H8ClNO. It is a derivative of benzamide, where a chlorine atom is attached to the nitrogen atom, and a methyl group is also present on the nitrogen atom. Benzamide, N-chloro-N-methyl- is a white crystalline solid and is used as a reagent in organic synthesis, particularly in the preparation of various benzene derivatives. It is also known for its use in the chloromethylation of amines, a process that introduces a chloromethyl group into an organic molecule. The compound is sensitive to light and moisture, and it is typically stored under controlled conditions to maintain its stability.

5014-48-2

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5014-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5014-48-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,1 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5014-48:
(6*5)+(5*0)+(4*1)+(3*4)+(2*4)+(1*8)=62
62 % 10 = 2
So 5014-48-2 is a valid CAS Registry Number.

5014-48-2Upstream product

5014-48-2Relevant academic research and scientific papers

Total Synthesis and Anti-Cancer Activity of All Known Communesin Alkaloids and Related Derivatives

Pompeo, Matthew M.,Cheah, Jaime H.,Movassaghi, Mohammad

, p. 14411 - 14420 (2019)

A unified enantioselective total synthesis and anticancer evaluation of all known epoxide-containing communesin alkaloids and related derivatives is described. Our synthesis is predicated on the convergent and modular diazene-directed assembly of two comp

t-butyl hypochlorite: A powerful electrophilic aromatic ring chlorinating agent

Lengyel, Istvan,Cesare, Victor,Stephani, Ralph

, p. 1891 - 1896 (1998)

t-Butyl hypochlorite is an excellent aromatic ring chlorinating agent, under mild conditions, without any catalyst, of acetanilide. High regioselectivity is observed, the product being, nearly exclusively, para- chloroacetanilide.

Convergent and Biomimetic Enantioselective Total Synthesis of (-)-Communesin F

Lathrop, Stephen P.,Pompeo, Matthew,Chang, Wen-Tau T.,Movassaghi, Mohammad

supporting information, p. 7763 - 7769 (2016/07/06)

The first biomimetic enantioselective total synthesis of (-)-communesin F based on a late-stage heterodimerization and aminal exchange is described. Our synthesis features the expedient diazene-directed assembly of two advanced fragments to secure the con

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