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3-methylthio-3-methyl-1-cyclobutanecarbonitrile is a complex organic compound with the molecular formula C7H11NS. It features a cyclobutane ring, which is a four-membered carbon ring, with a nitrile group (-CN) attached to one of the carbons. Additionally, it has two methyl groups (-CH3) and a methylthio group (-SCH3), which are both substituents on the cyclobutane ring. 3-methylthio-3-methyl-1-cyclobutanecarbonitrile is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through chemical reactions involving cyclobutane derivatives and is used as an intermediate in the production of certain drugs and pesticides. The compound's properties, such as its reactivity and stability, make it a valuable component in the development of new chemical entities.

5011-65-4

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5011-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5011-65-4 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 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5011-65:
(6*5)+(5*0)+(4*1)+(3*1)+(2*6)+(1*5)=54
54 % 10 = 4
So 5011-65-4 is a valid CAS Registry Number.

5011-65-4Downstream Products

5011-65-4Relevant academic research and scientific papers

REGIOSELECTIVITY OF THE ADDITION OF THIOLS TO 1-R-3-METHYLBICYCLOBUTANES

Vasin, V. A.,Razin, V. V.,Bolusheva, I. Yu.,Tanaseichuk, B. S.,Surmina, L. S.,Zefirov, N. S.

, p. 469 - 477 (2007/10/02)

The radical addition of thiols to 1-cyano-, 1-methoxycarbonyl-, 1-tert-butoxycarbonyl-, 1-acetyl-, and 1-benzoyl-3-methylbicyclobutanes was studied by GLC and PMR.In the case of thiophenol it was shown that the regioselectivity and relative reactivity of addition are determined by the polarity of the substituent.This is reflected in the satisfactory correlation between these values and the Taft ? constants.

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