1,2,3-1H-Triazole 288-36-8 CAS NO.288-36-8
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- Min.Order: 1 Kilogram
- Payment Terms: L/C,T/T
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A(10-150)Kilogram
- Product Details
Keywords
- 1,2,3-1H-Triazole 288-36-8
- 1,2,3-1H-Triazole 288-36-8
- 1,2,3-1H-Triazole 288-36-8
Quick Details
- ProName: 1,2,3-1H-Triazole 288-36-8
- CasNo: 288-36-8
- Molecular Formula: C2H3N3
- Appearance: Liquid
- Application: Organic Chemicals
- DeliveryTime: according to client's demand quantity
- PackAge: as requested
- Port: SHANGHAI
- ProductionCapacity: 100 Metric Ton/Day
- Purity: 99%
- Storage: room temperature
- Transportation: by sea
- LimitNum: 1 Kilogram
- Heavy metal: 0.01
- Grade: Industrial Grade,Pharma Grade
- Transportation: LCL
Superiority
Product Name: 1,2,3-1H-Triazole
Synonyms: 1, 2, 3-triazoles;LABOTEST-BB LT02056574;1H-1,2,3-TRIAZOLE;1,2,3-TRIAZOLE;1,2,3-1H-TRIAZOLE;TRIAZOLE(1,2,3-);1,2,3-Triazol;1H-1,2,3-Triazol
CAS: 288-36-8
MF: C2H3N3
MW: 69.07
EINECS: 608-262-3
Product Categories: Building Blocks;Heterocyclic Building Blocks;Triazoles;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File: 288-36-8.mol
1,2,3-1H-Triazole Chemical Properties
Melting point 23-25 °C(lit.)
Boiling point 203 °C752 mm Hg(lit.)
density 1.192 g/mL at 25 °C(lit.)
refractive index n20/D 1.498(lit.)
Fp 225 °F
storage temp. Refrigerator
pka 1.17(at 20℃)
form Liquid
color Clear colorless to yellow
Specific Gravity 1.192
Water Solubility soluble
BRN 104766
InChIKey QWENRTYMTSOGBR-UHFFFAOYSA-N
CAS DataBase Reference 288-36-8(CAS DataBase Reference)
NIST Chemistry Reference 1H-1,2,3-Triazole(288-36-8)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-63-36-22
Safety Statements 37/39-26-36/37
WGK Germany 3
Hazard Note Irritant
HS Code 29339900
1,2,3-1H-Triazole Usage And Synthesis
Description 1,2,3-1H-Triazole is a kind of azole compound. It can effectively promote the proton conduction in polymer electrolyte membranes via an intermolecular proton-transfer mechanism. It is also a useful triazole for proteomics research1. It also find use in research as a bioisostere in medicinal chemistry as well as an building block for more complex chemical compounds, including pharmaceutical drugs such as mubritinib and tazobactam2. It is a main class of hetero-cycles because of its extensive range of biological properties such as antimicrobial, anticancer, anti-tubercular, anti-HIV, antimalarial, antibacterial, antifungal, antiviral and anti-diabetic property3.
Details
Product Name: 1,2,3-1H-Triazole
Synonyms: 1, 2, 3-triazoles;LABOTEST-BB LT02056574;1H-1,2,3-TRIAZOLE;1,2,3-TRIAZOLE;1,2,3-1H-TRIAZOLE;TRIAZOLE(1,2,3-);1,2,3-Triazol;1H-1,2,3-Triazol
CAS: 288-36-8
MF: C2H3N3
MW: 69.07
EINECS: 608-262-3
Product Categories: Building Blocks;Heterocyclic Building Blocks;Triazoles;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File: 288-36-8.mol
1,2,3-1H-Triazole Chemical Properties
Melting point 23-25 °C(lit.)
Boiling point 203 °C752 mm Hg(lit.)
density 1.192 g/mL at 25 °C(lit.)
refractive index n20/D 1.498(lit.)
Fp 225 °F
storage temp. Refrigerator
pka 1.17(at 20℃)
form Liquid
color Clear colorless to yellow
Specific Gravity 1.192
Water Solubility soluble
BRN 104766
InChIKey QWENRTYMTSOGBR-UHFFFAOYSA-N
CAS DataBase Reference 288-36-8(CAS DataBase Reference)
NIST Chemistry Reference 1H-1,2,3-Triazole(288-36-8)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-63-36-22
Safety Statements 37/39-26-36/37
WGK Germany 3
Hazard Note Irritant
HS Code 29339900
1,2,3-1H-Triazole Usage And Synthesis
Description 1,2,3-1H-Triazole is a kind of azole compound. It can effectively promote the proton conduction in polymer electrolyte membranes via an intermolecular proton-transfer mechanism. It is also a useful triazole for proteomics research1. It also find use in research as a bioisostere in medicinal chemistry as well as an building block for more complex chemical compounds, including pharmaceutical drugs such as mubritinib and tazobactam2. It is a main class of hetero-cycles because of its extensive range of biological properties such as antimicrobial, anticancer, anti-tubercular, anti-HIV, antimalarial, antibacterial, antifungal, antiviral and anti-diabetic property3.