ChemicalBook > CAS DataBase List > N3-PhAc-OH

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
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N3-PhAc-OH Property

Melting point:
89-90 °C
form 
crystalline powder
color 
Yellow
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Safety

HS Code 
2929900090
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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.

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N-Bromosuccinimide Price

Iris Biotech GmbH
Product number
HAA2245
Product name
N3-PhAc-OH
Packaging
500mg
Price
$109.35
Updated
2021/12/16
Chem-Impex
Product number
30518
Product name
(4-Azidophenyl)aceticacid,≥99%(Assaybytitration,HPLC)
Purity
≥99%(Assaybytitration,HPLC)
Packaging
250MG
Price
$110.66
Updated
2021/12/16
Apolloscientific
Product number
BIBP1070
Product name
(4-azidophenyl)aceticacid
Purity
>99%
Packaging
250mg
Price
$118
Updated
2021/12/16
Oakwood
Product number
402247
Product name
2-(4-Azidophenyl)aceticacid
Packaging
1g
Price
$140
Updated
2021/12/16
Iris Biotech GmbH
Product number
HAA2245
Product name
N3-PhAc-OH
Packaging
1g
Price
$170.1
Updated
2021/12/16
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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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N3-PhAc-OH Suppliers

Alfa Chemistry
Tel
+1-5166625404;
Fax
1-516-927-0118
Email
Info@alfa-chemistry.com
Country
United States
ProdList
20405
Advantage
58
BOC Sciences
Tel
16314854226; +16314854226
Email
inquiry@bocsci.com
Country
United States
ProdList
19654
Advantage
58
Jilin Chinese Academy of Sciences-yanshen Technology
Tel
18143011203
Email
ET-market@chemextension.com
Country
China
ProdList
32048
Advantage
58
TargetMol Chemicals Inc.
Tel
15002134094
Email
marketing@targetmol.cn
Country
China
ProdList
29257
Advantage
58
Biosynth Biological Technology (Suzhou) Co Ltd
Tel
51288865780
Email
sales@biosynth.com
Country
China
ProdList
6051
Advantage
58

62893-37-2, N3-PhAc-OHRelated Search:


  • (4-Azidophenyl)acetic acid≥ 98% (HPLC)
  • N3-PhAc-OH
  • 2-(4-azidophenyl)acetic acid
  • (4-Azido-phenyl)-acetic acid
  • 62893-37-2