Thiophene-3-carboximidamide Hydrochloride

Base Information

• Chemical Name: Thiophene-3-carboximidamide Hydrochloride
• CAS No.: 51528-02-0
• Molecular Formula: C₅H₆N₂S*ClH
• Molecular Weight: 162.643
• Hs Code.: 2934999090
• European Community (EC) Number: 692-223-0
• DSSTox Substance ID: DTXSID60381504
• Mol file: 51528-02-0.mol

Synonyms:Thiophene-3-carboximidamide Hydrochloride;51528-02-0;3-Thiophenecarboximidamide hydrochloride;Thiophene-3-carboxamidine hydrochloride;thiophene-3-carboximidamide;hydrochloride;SCHEMBL3765931;DTXSID60381504;CAUZIIYPBLBRFI-UHFFFAOYSA-N;BCA52802;MFCD01940341;AKOS015996731;Thiophene-3-carboximidamideHydrochloride;CS-10919;CS-0258936;FT-0616408;EN300-71831;3-thiophenecarboximidamide hydrochloride, AldrichCPR;Z1266823180

Chemical Property of Thiophene-3-carboximidamide Hydrochloride

Chemical Property:

• Vapor Pressure: 0.111mmHg at 25°C
• Melting Point: 97 °C
• Boiling Point: 220.8°C at 760 mmHg
• Flash Point: 87.3°C
• PSA: 78.11000
• LogP: 2.63420
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 162.0018471
• Heavy Atom Count: 9
• Complexity: 103

Purity/Quality:

98%Min ^*data from raw suppliers

Thiophene-3-carboxamidinehydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xn
• Statements: 22-41
• Safety Statements: S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.; S37/39:Wear suitable g

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CSC=C1C(=N)N.Cl

Technology Process of Thiophene-3-carboximidamide Hydrochloride

There total 1 articles about Thiophene-3-carboximidamide Hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 64.0%

3-thiophenecarbonitrile (1641-09-4) → 3-amidinothiophene hydrochloride (51528-02-0)

Guidance literature:

With trimethylaluminum; ammonium chloride; In hexane; toluene; at 0 - 20 ℃; for 1.5h;

3-thiophenecarbonitrile; In hexane; toluene; at 80 ℃;

With methanol; In hexane; toluene; at 0 - 20 ℃;

upstream raw materials:

3-thiophenecarbonitrile

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