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(1Z,3Z)-1,4-Dichloro-1,3-butadiene is a chemical compound with the molecular formula C4H4Cl2. It is a colorless liquid with a pungent odor and is an isomer of 1,4-dichlorobutadiene. (1Z,3Z)-1,4-Dichloro-1,3-butadiene is characterized by two double bonds (Z configuration) between the first and third carbon atoms, and two chlorine atoms attached to the terminal carbons. It is used as an intermediate in the synthesis of various chemicals, such as pesticides and pharmaceuticals. Due to its reactivity and potential health hazards, it is important to handle (1Z,3Z)-1,4-Dichloro-1,3-butadiene with proper safety measures and in accordance with relevant regulations.

3588-11-2

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3588-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3588-11-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,8 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3588-11:
(6*3)+(5*5)+(4*8)+(3*8)+(2*1)+(1*1)=102
102 % 10 = 2
So 3588-11-2 is a valid CAS Registry Number.

3588-11-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name cis,cis-1,4-dichloro-1,3-butadiene

1.2 Other means of identification

Product number -
Other names cis,cis-1,4-Dichlor-1,3-butadien

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:3588-11-2 SDS

3588-11-2Downstream Products

3588-11-2Relevant academic research and scientific papers

Infrared multiphoton induced isomerization of cis-3,4-dichlorocyclobutene. I. Experimental results

Presser, Nathan,Mao, Chung-Rei,Moriarty, Robert M.,Gordon, Robert J.

, p. 6021 - 6029 (1983)

The yield and product distribution in the laser-induced isomerization of cis-3,4-dichlorocyclobutene (DCCB) have been measured as functions of laser fluence, DCCB pressure, and buffer gas pressure.Both Woodward-Hoffman allowed and "forbidden" isomers were observed.The fraction of "forbidden" products was found to increase linearly with fluence above a threshold of 3.5 J/cm2.At high fluence the yield increased quadratically with neat DCCB pressure.Both the yield and fraction of "forbidden" products declined monotonically with buffer gas pressure.These observations are explained in terms of a two-channel mechanism, in which the allowed isomer is formed in a concerted path and the forbidden isomers are produced from a diradical intermediate in a nonconcerted reaction.

1,4-Dilithio-1,3-butadlenes

Ashe III, Arthur J.,Mahmoud, Samir

, p. 1878 - 1880 (2008/10/08)

On treatment with (trimethylstannyl)lithium in THF at -78°C, 1,4-dichlorobutadienes (4) gave the stereoisomeric 1,4-bis(trimethylstannyl)-1,3-butadienes (5-7). Compounds 5 and 7 may be converted to the corresponding 1,4-dilithio-1,3-butadienes (1 and 3) by treatment with excess methyllithium, while 6 and 7 may be converted to 1 by reaction with 1 equiv of methyllithium.

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