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O-ISOPROPYLISOUREA HYDROCHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28811-41-8

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28811-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28811-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,1 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28811-41:
(7*2)+(6*8)+(5*8)+(4*1)+(3*1)+(2*4)+(1*1)=118
118 % 10 = 8
So 28811-41-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H10N2O.ClH/c1-3(2)7-4(5)6;/h3H,1-2H3,(H3,5,6);1H

28811-41-8SDS

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 O-ISOPROPYLISOUREA HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names Isopropoxyformamidin-hydrochlorid

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:28811-41-8 SDS

28811-41-8Relevant academic research and scientific papers

Process for the preparation of a 2-alkoxy-6-(trifluoromethyl)pyrimidin-4-ol

-

, (2008/06/13)

A novel process for the preparation of a 2-alkoxy-6-(trifluoromethyl)pyrimidin-4-ol of the general formula: STR1 in which R is a C1 -C8 -alkyl group. In the process, cyanamide is reacted with the appropriate alcohol in the presence of hydrogen chloride to give the corresponding alkoxyisourea hydrochloride, which is then converted with ethyl trifluoroacetoacetate in the presence of an alkali metal hydroxide, which is in water, to the end product of the formula I.

N and O-isopropyl isomers of barbital and phenobarbital: Physicochemical and pharmacological properties

Menez,Bourin,Colombel,et al.

, p. 521 - 529 (2007/10/02)

Univocal synthesis of O and N isopropylated derivatives of barbital and phenobarbital is proposed. Properties of those compounds in solution (pka and lipophilicity) show important differences. However the phenobarbital derivatives keep the anticonvulsant

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