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4270-00-2

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4270-00-2 Usage

General Description

Carbamimidothioic acid, bromide, pentyl ester is a chemical compound consisting of a carbamimidothioic acid molecule bonded to a pentyl ester with a bromide atom. Carbamimidothioic acid is a derivative of thiourea, containing a sulfur atom bonded to an amidine group, and is often used in the synthesis of various organic compounds. The presence of the bromide atom indicates that this compound contains a bromine ion, which can have various chemical properties and interactions. The pentyl ester group suggests that the carbamimidothioic acid molecule is esterified with a pentyl alcohol, which can affect its solubility and volatility. Overall, carbamimidothioic acid, bromide, pentyl ester is a complex chemical with potential applications in organic synthesis and other chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 4270-00-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4270-00:
(6*4)+(5*2)+(4*7)+(3*0)+(2*0)+(1*0)=62
62 % 10 = 2
So 4270-00-2 is a valid CAS Registry Number.

4270-00-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name S-pentyl-isothiourea

1.2 Other means of identification

Product number -
Other names S-n-pentylisothiourea

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:4270-00-2 SDS

4270-00-2Downstream Products

4270-00-2Relevant articles and documents

Synthesis of sulfides by reactions of 1,1-dichloro-2-chloro- methylcyclopropane with S-nucleophiles

Mikhed'kina,Nedel'ko,Prezhdo

, p. 370 - 375 (2007/10/03)

1,1-Dichloro-2-chloromethylcyclopropane reacts with thiolates to give 2,2-dichlorocyclopropylmethyl sulfides via replacement of the side-chain chlorine atom. The resulting sulfides are readily oxidized to the corresponding sulfones.

SYNTHESIS OF MONO(ALKYLTHIO)-SUBSTITUTED KETONES

Sabirov, S. S.,Gnevasheva, L. M.,Ismailov, M. I.,Isobaev, M. D.

, p. 1239 - 1243 (2007/10/02)

In the reaction of 2-propanone in the presence of sodium bicarbonate with a mixture of formaldehyde and the corresponding alkaline hydrolyzates of S-alkylthiuronium salts (thioalcoholates) β-keto sulfides (1-alkylthio-3-butanones) were obtained.Ketalization of the products with glycerol gave the cyclic derivatives alkylthio-1,3-dioxolanes.

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