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1,3-bis(1,3-benzodithiol-2-ylidene)urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84384-24-7

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84384-24-7 Usage

Family

Cyclophanes

Structure

Cyclic organic compound with alternating single and double bonds

Known for

Unique structure and potential applications in organic synthesis and materials science

Potential applications

a. Catalyst in various chemical reactions
b. Use in sensors and electronic devices
c. Investigated for potential anti-cancer properties

Importance

Diverse range of applications and unique structure make it an interesting and significant compound in the field of chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 84384-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,8 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 84384-24:
(7*8)+(6*4)+(5*3)+(4*8)+(3*4)+(2*2)+(1*4)=147
147 % 10 = 7
So 84384-24-7 is a valid CAS Registry Number.

84384-24-7SDS

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 1,3-bis(1,3-benzodithiol-2-ylidene)urea

1.2 Other means of identification

Product number -
Other names -

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:84384-24-7 SDS

84384-24-7Downstream Products

84384-24-7Relevant academic research and scientific papers

About the Preparation and Chlorination of Carbonyl Diisothiocyanate

Bunnenberg, Rolf,Jochims, Johannes C.,Haerle, Helmut

, p. 3587 - 3596 (2007/10/02)

An improved preparation of carbonyl diisothiocyanate (1) is described.Compound 1 can be stored in form of its stable hydrochloride 3.Depending on the reaction conditions chlorination of 1 leads to the acyl isocyanide dichlorides 5 or 8.Compound 5 reacts with amines to give: the triazines 9a - c, the ammelines 11a, b, the guanidines 12 and 16a, or the acylcarbodiimides 14 and 15.With sodium phenolate 5 forms the dialkylidene urea 17, and with thiolates the derivatives 18a - c of dithiocarbonic acid.Compound 8 racts with thiophenolate to give 19 and with tert-butylamine to yield the carbamoylcarbodiimide 20.

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