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1-Chloro-1-methyl-2-nitrosocyclohexane is a chemical compound with the molecular formula C7H12ClNO2. It is a derivative of cyclohexane, a cyclic hydrocarbon, with a chlorine atom attached to one carbon atom, a methyl group (CH3) attached to the adjacent carbon atom, and a nitroso group (NO) attached to the carbon atom opposite the chlorine. 1-chloro-1-methyl-2-nitrosocyclohexane is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions, such as the nitrosation of 1-chloro-1-methylcyclohexane, and can undergo further reactions to form a variety of products. The compound is sensitive to light and heat, and should be stored and handled with care to prevent decomposition or unwanted side reactions.

4358-03-6

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4358-03-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4358-03-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,5 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4358-03:
(6*4)+(5*3)+(4*5)+(3*8)+(2*0)+(1*3)=86
86 % 10 = 6
So 4358-03-6 is a valid CAS Registry Number.

4358-03-6Upstream product

4358-03-6Relevant academic research and scientific papers

Specific Inhibitors in Vitamin Biosynthesis. Part 7. Syntheses of Blocked 7,8-Dihydropteridines via &α-Amino Ketones

Al-Hassan, Saiba S.,Cameron, Robert J.,Curran, Adrian W. C.,Lyall, William J. S.,Nicholson, Sydney H.,et al.

, p. 1645 - 1660 (2007/10/02)

The synthesis of 15 blocked 7,8-dihydropteridines is described in which the pyrazine ring is built from a derivative of an α-amino ketone.Three routes to the amino ketones based upon amino acids, nitrosyl chloride addition to alkenes, and nitro alcohols are discussed.The compounds synthesised are inhibitors of 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase , an enzyme in the pathway leading to dihydrofolate, and the inhibitory potencies of the compounds are discussed in the light of a hypothetical active site model for the enzyme.

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