N3-PhAc-OH
- Product Name
- N3-PhAc-OH
- CAS No.
- 62893-37-2
- Chemical Name
- N3-PhAc-OH
- Synonyms
- N3-PhAc-OH;(4-Azido-phenyl)-acetic acid;2-(4-azidophenyl)acetic acid;(4-Azidophenyl)acetic acid≥ 98% (HPLC)
- CBNumber
- CB13333867
- Molecular Formula
- C8H7N3O2
- Formula Weight
- 177.16008
- MOL File
- 62893-37-2.mol
N3-PhAc-OH Property
- Melting point:
- 89-90 °C
- form
- crystalline powder
- color
- Yellow
Safety
- HS Code
- 2929900090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- HAA2245
- Product name
- N3-PhAc-OH
- Packaging
- 500mg
- Price
- $109.35
- Updated
- 2021/12/16
- Product number
- 30518
- Product name
- (4-Azidophenyl)aceticacid,≥99%(Assaybytitration,HPLC)
- Purity
- ≥99%(Assaybytitration,HPLC)
- Packaging
- 250MG
- Price
- $110.66
- Updated
- 2021/12/16
- Product number
- BIBP1070
- Product name
- (4-azidophenyl)aceticacid
- Purity
- >99%
- Packaging
- 250mg
- Price
- $118
- Updated
- 2021/12/16
- Product number
- 402247
- Product name
- 2-(4-Azidophenyl)aceticacid
- Packaging
- 1g
- Price
- $140
- Updated
- 2021/12/16
- Product number
- HAA2245
- Product name
- N3-PhAc-OH
- Packaging
- 1g
- Price
- $170.1
- Updated
- 2021/12/16
N3-PhAc-OH Chemical Properties,Usage,Production
Chemical Properties
Yellow crystalline powder
Uses
N3-PhAc-OH is a click chemistry reagent containing an azide group. Click chemistry has great potential for use in binding between nucleic acids, lipids, proteins, and other molecules, and has been used in many research fields because of its beneficial characteristics, including high yield, high specificity, and simplicity[1]. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.
References
[1] Jiang X, et al. Recent applications of click chemistry in drug discovery. Expert Opin Drug Discov. 2019 Aug;14(8):779-789. DOI:10.1080/17460441.2019.1614910
N3-PhAc-OH Preparation Products And Raw materials
Raw materials
Preparation Products
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