124638-99-9

Basic information

• Product Name: 1H-1,2,4-Triazole-3,5-diamine, 1-dodecyl-
• CAS NO: 124638-99-9
• Molecular Formula: C14H29N5
• Molecular Weight: 267.418
• Mol File: 124638-99-9.mol

Chemical Properties

• CAS DataBase Reference: 1H-1,2,4-Triazole-3,5-diamine, 1-dodecyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,4-Triazole-3,5-diamine, 1-dodecyl-(124638-99-9)
• EPA Substance Registry System: 1H-1,2,4-Triazole-3,5-diamine, 1-dodecyl-(124638-99-9)

Safety Data

• Hazardous Substances Data: 124638-99-9(Hazardous Substances Data)

Usage

Molecular Weight

348.52 g/mol
The mass of one mole of the compound.

Chemical Family

Triazole Derivatives
A group of chemical compounds that share a common 1,2,4-triazoles core structure.

Common Uses

Synthesis of Pharmaceuticals, Agrochemicals, and Dyes
Acts as an intermediate in the production of various chemical products.

Additional Uses

Corrosion Inhibitor, Stabilizer, and Polymer Component
Utilized in material protection and enhancement.

Potential Applications

Biomedical Research
Possesses antifungal and antimicrobial properties for possible use in medical applications.

Hazardous Nature

Considered a Hazardous Chemical
Requires proper handling, safety, and storage protocols to minimize risks.

Safety and Handling Precautions

Follow Proper Protocols
Ensure that appropriate measures are taken to protect individuals and the environment from potential hazards.

Upstream product

• 1455-77-2 guanazole 
• 143-15-7 1-dodecylbromide 
• 1455-77-2 guanazole 

Relevant articles and documents

Solution-processable conjugated polymers containing alternating 1-alkyl-1,2,4-triazole and N=S=N links

Poly(sulfur nitride), [SN]x, is an infinite π-bonded system and only known polymeric superconductor composed of nonmetallic elements. The appealing electronic properties of [SN]x, along with the safety issue involved in the synthesis

Phthalocyanine Analogues. Part 1. Synthesis, Spectroscopy, and Theoretical Study of 8,18-Dihydrodibenzo-5,7,8,10,15,17,18,20-octa-azaporphyrin and MNDO Calculations on its Related Hueckel Heteroannulene

Three hemiporphyrazines containing two 1,2,4-triazole subunits, namely the N,N'-unsubstituted, the N,N'-didodecyl-, N,N'-diphenyl-substituted derivatives, have been synthetised and fully characterized (m. s., u. v., and n. m. r.).In particular, high-resolution solid-state 13C n. m. r. spectroscopy has proved to be a suitable method for the study of this highly insoluble class of compounds, giving valuable information on their tautomerism.An MNDO theoretical study (fully optimized geometries) has been carried out in order to understand why the didehydro derivative (7) (an 18?-electron aromatic porphyrin) is much less stable than the corresponding N,N'-unsubstituted hemiporphyrazine (6).The explanation lies in the peculiar structure of 1,2,4-triazoline-3,5-di-imine that one triazoline ring of (7) must adopt in order to allow a fully conjugated system.This structure has also been calculated, and shows a strong tendency to lose bound fragments (molecular dinitrogen and the azomethyne ylide HN=C+-NH-C-=NH).