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Hexahydrobenzohydroxamoyl chloride, also known as 1,4-cyclohexanedimethanamine hydrochloride, is an organic compound with the chemical formula C8H16ClNO. It is a white crystalline solid that is soluble in water and slightly soluble in ethanol. hexahydrobenzohydroxamoyl chloride is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its use in the production of certain dyes and pigments. The compound is synthesized through the reaction of cyclohexane with formaldehyde and ammonia, followed by the addition of hydrochloric acid to form the hydrochloride salt. Due to its reactivity, hexahydrobenzohydroxamoyl chloride is often used in the formation of amide and urea linkages in chemical reactions, making it a versatile building block in the creation of complex organic molecules.

2987-32-8

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2987-32-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2987-32-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2987-32:
(6*2)+(5*9)+(4*8)+(3*7)+(2*3)+(1*2)=118
118 % 10 = 8
So 2987-32-8 is a valid CAS Registry Number.

2987-32-8Relevant academic research and scientific papers

Preparation of N-chloroamides using trichloroisocyanuric acid

Hiegel, Gene A.,Hogenauer, Tyrone J.,Lewis, Justin C.

, p. 2099 - 2105 (2005)

Amides are efficiently converted to N-chloroamides by trichloroisocyanuric acid in methanol. Copyright Taylor & Francis, Inc.

Preparation of methyl N-substituted carbamates from amides through N-chloroamides

Hiegel, Gene A.,Hogenauer, Tyrone J.

, p. 2091 - 2098 (2007/10/03)

Amides are chlorinated on the nitrogen using trichloroisocyanuric acid, and the N-chloroamides are then rearranged to the corresponding methyl N-substituted carbamates by sodium methoxide in methanol. Copyright Taylor & Francis, Inc.

BEHAVIOUR OF NITRILE OXIDES TOWARDS NUCLEOPHILES. VI. SYNTHESIS AND POLYMERIZATION OF ALIPHATIC NITRILE OXIDES

Sarlo, Francesco De,Guarna, Antonio,Brandi, Alberto,Mascagni, Paolo

, p. 341 - 344 (2007/10/02)

Some new aliphatic nitrile oxides have been prepared and allowed to react with pyridine or trimethylamine in ethanol: as for acetonitrile oxide, they undergo polymerization to cyclic oligomers or higher polymers.Linking of monomer units through C-O bonds

SYNTHESIS OF ALIPHATIC ISOCYANATES VIA A TWO-PHASE HOFMANN REACTION

Sy, Anita O.,Raksis, Joseph W.

, p. 2223 - 2226 (2007/10/02)

A convenient method of preparing aliphatic isocyanates via a two-phase Hofmann reaction using a phase transfer catalyst is described.

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