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5-(Chloromethyl)-6-propyl-1,3-benzodioxole is an organic chemical compound characterized by a benzodioxole ring, which is a benzene ring with two oxygen atoms forming a dioxole group. The molecule features a chloromethyl group (-CH2Cl) at the 5-position and a propyl chain (-CH2CH2CH3) at the 6-position. 5-(Chloromethyl)-6-propyl-1,3-benzodioxole is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It can participate in a range of chemical reactions, such as nucleophilic substitutions, due to the presence of the electrophilic chlorine atom. The compound's properties, such as its boiling point, solubility, and stability, can be influenced by the presence of these functional groups, making it a versatile building block in organic synthesis.

1938-32-5

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1938-32-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1938-32-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,3 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1938-32:
(6*1)+(5*9)+(4*3)+(3*8)+(2*3)+(1*2)=95
95 % 10 = 5
So 1938-32-5 is a valid CAS Registry Number.

1938-32-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(chloromethyl)-6-propyl-1,3-benzodioxole

1.2 Other means of identification

Product number -
Other names 6-chloromethyl-dihydrosafrol

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:1938-32-5 SDS

1938-32-5Relevant academic research and scientific papers

AN EFFICIENT AND ENVIRONMENT FRIENDLY PROCESS FOR CHLOROMETHYLATION OF SUBSTITUTED BENZENES

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Paragraph 0075; 0080, (2020/12/30)

Disclosed herein is an efficient, environment friendly and commercially viable process for preparation of chloromethylated compound of formula I in substantially pure form and high yield, from the compound of formula II. The process includes contacting the compound of formula II with a chloromethylating agent generated in-situ by reaction of a formaldehyde precursor and hydrogen chloride, in a suitable solvent/contacting medium and in the presence of a catalytic amount of a short chain/low molecular weight carboxylic acid of formula III. I II III wherein, R1, R2, R3 and R4 are as defined in the description.

Synthetic and mechanistic investigation of piperonyl butoxide from dihydrosafrole

Wang, Shuai,Liu, Jinqiang,Qian, Chao,Chen, Xinzhi

experimental part, p. 147 - 160 (2012/05/20)

Piperonyl butoxide (PBO) 1 was prepared via the successive chloromethylation and etherification of dihydrosafrole 3. In this work, during the chloromethylation of 3, several by-products such as 5 (the isomer of chloromethyldihydrosafrole 4), 6-propylpiperonyl alcohol 6, bis(chloromethyl)- dihydrosafrole 7 and 8, bis(2-propyl-4,5-methylenedioxyphenyl)methane 9 and di(2-propyl-4,5-methy lene-dioxybenzyl)ether 10 were found. However, it was found that 5, 6, 7, and 8 could undergo a further reaction to the final product (PBO), rather than its derivatives, though the by-products 9 and 10 still existed. Based on these results, the plausible mechanism of the chloromethylation and etherification of 3 was proposed. Furthermore, the reliability of the plausible mechanism was verified by quantum chemical calculations using DFT. In addition, the final product (PBO) was produced with a high selectivity and yield by reducing the by-products 9 and 10. Springer Science+Business Media B.V. 2011.

Benzodioxale derivatives

-

, (2008/06/13)

A new benzodioxole derivative has a substituent in the phenyl ring which is a carboxyalkylthioalkyl or the like and is effective to treat a liver disease.

Synergistic arthropodicidal compositions and methods of use

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, (2008/06/13)

A synergistic arthropodicidal composition comprising (a) a benzodioxole derivative of the formula STR1 in which R represents alkyl, alkenyl, alkynyl, aryl or aralkyl, plus (b) at least one compound selected from (A) carbamates, (B) carboxylic acid esters, (C) phosphoric and phosphonic acid esters and (D) halogenoalkanes, and its use in combating arthropods.

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