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((2R,3R)-1-Chloro-2,3-dimethyl-cyclopropyl)-benzene is a chiral organic compound characterized by its unique structure. It features a cyclopropane ring with two methyl groups at the 2 and 3 positions, both in the R configuration, and a chlorine atom at the 1 position. This cyclopropyl group is attached to a benzene ring, which is a planar, aromatic structure consisting of six carbon atoms in a hexagonal arrangement with alternating double bonds. The compound's chirality arises from the presence of the two methyl groups on the cyclopropane ring, which can exist in two enantiomeric forms. This specific compound is one of the enantiomers, with the R configuration at both the 2 and 3 positions. The presence of the chlorine atom and the cyclopropane ring make ((2R,3R)-1-Chloro-2,3-dimethyl-cyclopropyl)-benzene potentially useful in various chemical reactions and applications, such as in the synthesis of pharmaceuticals or other specialty chemicals.

13153-99-6

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13153-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13153-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,5 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13153-99:
(7*1)+(6*3)+(5*1)+(4*5)+(3*3)+(2*9)+(1*9)=86
86 % 10 = 6
So 13153-99-6 is a valid CAS Registry Number.

13153-99-6Downstream Products

13153-99-6Relevant academic research and scientific papers

A PHENYLCARBENE TRANSFER SYSTEM

Cunico, Robert F.,Chu, Kuang S.

, p. 271 - 278 (2007/10/02)

Treatment of (α,α-dichlorobenzyl)trimethylsilane with potassium fluoride/18-crown-6 ether/diglyme transfers phenylchlorocarbene to a number of carbenophiles at room temperature.

MECHANISM OF C-H INSERTION OF CARBENE IN RIGID MATRIX

Tomioka, Hideo,Ozaki, Yasuji,Izawa, Yasuji

, p. 843 - 846 (2007/10/02)

C-H insertion process of phenylchlorocarbene, a ground state singlet carbene, is not affected by matrix which generally exerts its effect in C-H insertion of most arylcarbenes.This reveals the origin of the matrix effects on carbene reactions.

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