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1-Propene, 1,3-dichloro-2-methyl-, (E)-, also known as (E)-1,3-dichloro-2-methylprop-1-ene, 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 two chlorine atoms attached to the first and third carbon atoms, respectively. 1-Propene, 1,3-dichloro-2-methyl-, (E)- is an isomer of 1,3-dichloro-2-methylpropene, with the difference being the geometric arrangement of the chlorine atoms around the double bond. The (E)-isomer has the chlorine atoms on the same side of the double bond, while the (Z)-isomer has them on opposite sides. 1-Propene, 1,3-dichloro-2-methyl-, (E)- is used as an intermediate in the synthesis of various chemicals and pharmaceuticals, and it is important to handle it with care due to its potential toxicity and environmental impact.

35329-41-0

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35329-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35329-41-0 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 35329-41:
(7*3)+(6*5)+(5*3)+(4*2)+(3*9)+(2*4)+(1*1)=110
110 % 10 = 0
So 35329-41-0 is a valid CAS Registry Number.

35329-41-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1,3-Dichloro-2-methyl-1-propene

1.2 Other means of identification

Product number -
Other names E-1,3-dichloro-2-methyl-1-propene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:35329-41-0 SDS

35329-41-0Downstream Products

35329-41-0Relevant 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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