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1-Propene, 1,3-dichloro-2-methyl-, (Z)-, also known as (Z)-1,3-dichloro-2-methylpropene, is an organic compound with the chemical formula C4H6Cl2. It is a colorless liquid with a pungent odor and is characterized by the presence of a double bond between the first and third carbon atoms in the propene chain, with a methyl group attached to the second carbon and two chlorine atoms attached to the first and third carbons. 1-Propene, 1,3-dichloro-2-methyl-, (Z)- is a valuable intermediate in the synthesis of various chemicals, such as pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive nature, it is important to handle 1-Propene, 1,3-dichloro-2-methyl-, (Z)- with care, as it can be toxic and harmful to the environment.

35329-40-9

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35329-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35329-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,2 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35329-40:
(7*3)+(6*5)+(5*3)+(4*2)+(3*9)+(2*4)+(1*0)=109
109 % 10 = 9
So 35329-40-9 is a valid CAS Registry Number.

35329-40-9Downstream Products

35329-40-9Relevant academic research and scientific papers

Synthesis and Characterization of Polychlorinated Isobutenes

Schulze, K.,Hartmann, S.,Krueger, H.,Muehlstaedt, M.,Richter, C.,Richter, H.

, p. 433 - 442 (2007/10/02)

The preparation of polychlorinated methallylic chlorides by continuous chlorination of isobutene with different ratios of chlorine and following HCl-elimination is described.The structure is proved by reaction of the polychlorinated isobutenes with sodium thiolacetate and potassium thiocyanate and by spectroscopic methods.

REACTIONS OF CHLORINE MONOFLUORIDE. IV. ADDITION OF CHLORINE MONOFLUORIDE TO HALOGEN-SUBSTITUTED ALKENES

Boguslavskaya, L. S.,Chuvatkin, N. N.,Panteleeva, I. Yu.

, p. 1832 - 1842 (2007/10/02)

The reactions of chlorine monofluoride with halogenoethylenes (1,1-dichloro-, 1,2-dichloro-, trichloro-, and tetrachloroethylenes) and halogenopropenes ( 3-bromo-, 3,3,3-trichloro-, E- and Z-1,3-dichloro-, 3-chloro-2-methyl-, and perfluoropropenes) were investigated in inert solvents in the presence of ethyl acetate as external nucleophile.In all cases chloroacyloxy adducts were isolated and identified in addition to the chlorofluorination products, and this indicates an electrophilic mechanism for the chlorofluorination of polyhalogenoalkenes.Methyl chloromaleate, chlorofumarate, chlorofluoroethylenedicarboxylate, α,β-difluoroacrylate, and perfluoromethacrylate in anhydrous hydrogen fluoride form the corresponding chlorofluoro adducts with satisfactory yields, whereas the reaction takes place with difficulty in inert solvents.

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