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Carbamimidic acid, (aminoiminomethyl)-, methyl ester, monohydrochloride is a chemical compound with the molecular formula C3H8N2O2.HCl. It is an ester derivative of carbamimidic acid, featuring an amino group attached to the imino group, and a methyl group esterifying the carboxylic acid moiety. Carbamimidic acid, (aminoiminomethyl)-, methyl ester, monohydrochloride is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides and drugs. The presence of the hydrochloride salt indicates that it is a salt form of the parent compound, which can affect its solubility and reactivity in different chemical processes.

869-75-0

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869-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 869-75-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,6 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 869-75:
(5*8)+(4*6)+(3*9)+(2*7)+(1*5)=110
110 % 10 = 0
So 869-75-0 is a valid CAS Registry Number.

869-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name guanyl-O-methylisourea hydrochloride

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:869-75-0 SDS

869-75-0Upstream product

869-75-0Relevant academic research and scientific papers

Process for the preparation of 2-amino-s-triazines

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, (2008/06/13)

The present invention relates to a process for the preparation of 2-amino-s-triazines in three stages. In the first stage nitriles, alcohols and hydrogen chloride are reacted to form the corresponding imido-ester hydrochlorides. In the second stage, the imido-ester hydrochlorides are reacted with cyanamide in the aqueous phase to form the N-cyanimido-esters, which comprises carrying out the first stage in the presence of acetic acid esters and the second stage in an aqueous solution which has been brought to a pH value of 5-8 by addition of bases, and reacting the N-cyanimido-esters with O-alkylisourea, S-alkylisothiourea, guanidine or amidine salts in the presence of a base in the third stage. The 2-amino-s-triazines can be prepared in a high purity and with good yields in this manner.

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