4-Aminobenzamidine dihydrochloride

• CAS: 2498-50-2
• Catalog Number: ACM2498502
• Category: Other Products
• Molecular Weight: 208.09
• Molecular Formula: C₇H₁₁Cl₂N₃
• Synonyms: 4-AMINOBENZAMIDINE DIHYDROCHLORIDE;4-AMINOBENZAMIDINE HCL SALT;BENZENECARBOXIMIDAMIDE, 4-AMINO-, DIHYDROCHLORIDE;P-AMINOBENZAMIDINE DIHCL;P-AMINOBENZAMIDINE DIHYDROCHLORIDE;4-amino-benzenecarboximidamiddihydrochloride;4-aminobenzenecarboximidamidedihydrochloride;p-amino-benzamidindihydrochloride
• Melting Point: >300°C(lit.)
• Hazard Statements: Xi,Xn
• Safety Description: 26-37/39-36
• Supplemental Hazard Statements: H315-H319-H335
• Symbol: GHS07

Custom Q&A

What is the PubChem CID for 4-Aminobenzamidine dihydrochloride?

PubChem CID 75626.

What is the molecular formula of 4-Aminobenzamidine dihydrochloride?

The molecular formula is C7H11Cl2N3.

What is the molecular weight of 4-Aminobenzamidine dihydrochloride?

The molecular weight is 208.09 g/mol.

What is the IUPAC name of 4-Aminobenzamidine dihydrochloride?

The IUPAC name is 4-aminobenzenecarboximidamide;dihydrochloride.

What is the InChI key of 4-Aminobenzamidine dihydrochloride?

The InChI key is GHEHNICLPWTXJC-UHFFFAOYSA-N.

What is the Canonical SMILES of 4-Aminobenzamidine dihydrochloride?

The Canonical SMILES is C1=CC(=CC=C1C(=N)N)N.Cl.Cl.

What is the CAS number of 4-Aminobenzamidine dihydrochloride?

The CAS number is 2498-50-2.

How many hydrogen bond donor count does 4-Aminobenzamidine dihydrochloride have?

It has 5 hydrogen bond donor counts.

How many rotatable bond count does 4-Aminobenzamidine dihydrochloride have?

It has 1 rotatable bond count.

What is the topological polar surface area of 4-Aminobenzamidine dihydrochloride?

The topological polar surface area is 75.9 ?2.

Synthetic Use

Upstream Synthesis Route 1

• 25412-75-3

• 2498-50-2

Reference: [1] Patent: CN104163778, 2016, B, . Location in patent: Paragraph 0056; 0057

Upstream Synthesis Route 2

• 873-74-5

• 2498-50-2

Reference: [1] Patent: WO2014/64016, 2014, A1,

Upstream Synthesis Route 3

• 619-72-7

• 2498-50-2

Reference: [1] Patent: CN104163778, 2016, B,

Downstream Synthesis Route 1

• 65465-66-9
• 2498-50-2

• 133118-43-1

Reference: [1]European Journal of Medicinal Chemistry,1990,vol. 25,p. 673 - 680

* For details of the synthesis route, please refer to the original source to ensure accuracy.