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c-4-iodo-t-3-thiocyanato-r-1-t-butylcyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74741-10-9

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74741-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74741-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,4 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74741-10:
(7*7)+(6*4)+(5*7)+(4*4)+(3*1)+(2*1)+(1*0)=129
129 % 10 = 9
So 74741-10-9 is a valid CAS Registry Number.

74741-10-9Relevant academic research and scientific papers

vic-Iodothiocyanates and Iodoisothiocyanates. Part 3. Further Preperations, and the Formation of 2-Alkoxy-2-thiazolines

Cambie, Richard C.,Chambers, David,Rutledge, Peter S.,Woodgate, Paul D.,Woodgate, Shella D.

, p. 33 - 39 (2007/10/02)

The reactions of (E)-hex-3-ene, 4-t-butylcyclohexene, and 3-t-butylcyclohexene with iodine and potassium thiocyanate are examined.The action of iodine and thiocyanogen with (E)-hex-3-ene gives different results from those reported in the literature.Isomerization of the vic-iodothiocyatates and formation of 2-alkoxy-2-thiazolines from the latter adducts are reported.

Oxidative Displacement of Hypervalent Iodine from Alkyl Iodides

Cambie, Richard C.,Chambers, David,Lindsay, Barry G.,Rutledge, Peter S.,Woodgate, Paul D.

, p. 822 - 827 (2007/10/02)

Oxidative displacement of iodine from primary alkyl iodides and vic-substituted iodocyclohexanes with m-chloroperbenzoic acid in either dichloromethane or t-butyl alcohol-water gives primary alcohols and vic-substituted cyclohexanols, respectively.Retention of configuration at the displacement centre occurs for all of the trans-vic-substituted iodocyclohexanes except the iodoacetate and iodotrifluoroacetate where inversion of configuration occurs to give cis-hydroxy-esters.Oxidation of (S)-2-iodo-octane occurs with almost complete inversion to give (R)-octan-2-ol but also affords octan-1-ol, octan-3-ol, and octan-2-one.

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