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16694-46-5

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16694-46-5 Usage

Description

Ethyl Formimidate Hydrochloride is a nitrogen-containing organic building block that serves as a versatile intermediate in various chemical syntheses. It is known for its ability to undergo degradation upon heating, yielding formamidine hydrochloride, ethyl formate, and ethyl chloride.

Uses

Used in Chemical Synthesis:
Ethyl Formimidate Hydrochloride is used as a building block for the preparation of s-triazines, 2,3:5,6-di-O-isopropylidene-αand -β-5-amino-4-ethoxycarbonyl or -carbamoyl-imidazole D-mannofuranosides. It plays a crucial role in the synthesis of complex organic compounds and pharmaceuticals.
Used in Pharmaceutical Industry:
Ethyl Formimidate Hydrochloride is used as a reactant in the synthesis of biologically active molecules, including Bredinin via amination of an acyclic precursor. ETHYL FORMIMIDATE HYDROCHLORIDE has therapeutic properties and is valuable in the development of new drugs.
Used in Antifungal Drug Synthesis:
In the pharmaceutical industry, Ethyl Formimidate Hydrochloride is also used as a reactant in the synthesis of Amidine conjugates of the ornithine moiety of an antifungal. This application highlights its importance in creating compounds with potential antifungal properties.
Used in Organic Chemistry Research:
Ethyl Formimidate Hydrochloride is utilized as a reactant involved in intermolecular cyclization and Mo-catalyzed asymmetric ring-closing metathesis for the synthesis of cyclid amides and amines. These processes are essential for the development of novel organic compounds with unique properties.
Used in Peptide Synthesis:
In the field of peptide chemistry, Ethyl Formimidate Hydrochloride is used in the synthesis of peptidic 1-cyanopyrrolidines. This application demonstrates its versatility in the creation of diverse peptide structures with potential biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 16694-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,9 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16694-46:
(7*1)+(6*6)+(5*6)+(4*9)+(3*4)+(2*4)+(1*6)=135
135 % 10 = 5
So 16694-46-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H7NO/c1-2-5-3-4/h3-4H,2H2,1H3/b4-3+

16694-46-5 Well-known Company Product Price

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  • Aldrich

  • (396788)  Ethylformimidatehydrochloride  

  • 16694-46-5

  • 396788-10G

  • 656.37CNY

  • Detail

16694-46-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl methanimidate,hydrochloride

1.2 Other means of identification

Product number -
Other names O-ethyl formimidate hydrochloride

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:16694-46-5 SDS

16694-46-5Relevant articles and documents

METHOD FOR PREPARING 5-CHLORO-N-(METHYL)THIOPHEN-2-CARBOXAMIDE DERIVATIVE AND INTERMEDIATE USED THEREIN

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Page/Page column 8, (2012/06/16)

Disclosed are: a method for preparing a 5-chloro-N-({(5S)-2-oxo-3-[4-(5,6-dihydro-4H-[1,2,4]triazin-1-yl)phenyl]-1,3-oxazolidin-5-yl}-methyl)thiophene-2-carboxamide derivative, which is a inhibitor of blood coagulation factor Xa, in a high purity and yiel

HETEROCYCLIC AMIDE COMPOUNDS AND PHARMACEUTICAL USE OF THE SAME

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, (2008/06/13)

Heterocyclic amide compounds of the formula (I) STR1 wherein each symbol is as defined in the specification, pharmacologically acceptable salts thereof, pharmaceutical compositions thereof and pharmaceutical use thereof. The heterocyclic amide compounds and pharmacologically acceptable salts thereof of the present invention have superior inhibitory activity against chymase groups in mammals inclusive of human, and can be administered orally or parenterally. Therefore, they are useful as chymase inhibitors and can be effective for the prophylaxis and treatment of various diseases caused by chymase, such as those caused by angiotensin II.

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