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Cyclohexylethylcarbamoyl chloride, also known as CXECC, is a chemical compound with the molecular formula C9H16ClNO. It is a carbamoyl chloride, which is a class of organic compounds that contain a carbamoyl functional group and a chloride group. CXECC is commonly used in the synthesis of pharmaceuticals and agricultural chemicals. It is a reactive intermediate that is often used as a building block in the production of various organic compounds. CXECC is a colorless to pale yellow liquid with a pungent odor, and it is highly corrosive and toxic, requiring careful handling and storage.

62899-75-6

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62899-75-6 Usage

Uses

Used in Pharmaceutical Industry:
Cyclohexylethylcarbamoyl chloride is used as a building block for the synthesis of various pharmaceutical compounds. Its reactive nature allows for the formation of amide bonds, which are essential in the structure of many drugs.
Used in Agricultural Chemical Industry:
Cyclohexylethylcarbamoyl chloride is used as a key intermediate in the production of agricultural chemicals. Its ability to form stable bonds with other molecules makes it a valuable component in the development of effective pesticides and herbicides.
Used in Organic Synthesis:
Cyclohexylethylcarbamoyl chloride is used as a reactive intermediate in the synthesis of various organic compounds. Its carbamoyl functional group and chloride group enable the formation of a wide range of chemical structures, making it a versatile building block in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 62899-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,9 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62899-75:
(7*6)+(6*2)+(5*8)+(4*9)+(3*9)+(2*7)+(1*5)=176
176 % 10 = 6
So 62899-75-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H16ClNO/c1-7(11-9(10)12)8-5-3-2-4-6-8/h7-8H,2-6H2,1H3,(H,11,12)

62899-75-6Relevant academic research and scientific papers

Use of C,N-chelated di-n-butyltin(IV) fluoride for the synthesis of acyl fluorides, fluoroformates and fluorophosgene

?vec, Petr,Eisner, Ale?,Kolá?ová, Lenka,Weidlich, Tomá?,Pejchal, Vladimír,R??i?ka, Ale?

body text, p. 6320 - 6323 (2009/04/06)

{2-[(CH3)2NCH2]C6H4}(n-Bu)2SnF (1) reacts with various chloroformates, acyl chlorides, methanesulfonyl chloride, 4,4′-dimethoxytrityl chloride and phosgene precursors or derivatives to form fluorinated analogues. All reactions proceed rapidly and under mild conditions. The use of a catalytic amount of 1 and KF in toluene led to a relatively high yield of a selected fluoroformate.

Process for the preparation of 1-4-disubstituted-5 (4H)-tetrazolinones

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, (2008/06/13)

1,4-Disubstituted-5(4H)-tetrazolinones of the formula (I) STR1 wherein R1, R2 and R3 have the meanings given in the specification), which are known to be useful as herbicides, can be obtained in very good yields by reacting the corresponding 1-substituted-5(4H)-tetrazolinones with the corresponding carbamoyl chlorides in the presence of 4-dimethylaminopyridine.

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