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1 G
CZK 1,310.00
About This Item
Linear Formula:
C6H5C6H4CH2NH2
CAS Number:
Molecular Weight:
183.25
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
mp
48-53 °C (lit.)
functional group
amine
phenyl
SMILES string
NCc1ccc(cc1)-c2ccccc2
InChI
1S/C13H13N/c14-10-11-6-8-13(9-7-11)12-4-2-1-3-5-12/h1-9H,10,14H2
InChI key
RMSPOVPGDBDYKH-UHFFFAOYSA-N
Related Categories
1 of 3
This Item | 661295 | 767794 |
|---|---|---|
| assay 97% | assay 97% | assay 97% |
| Quality Level 100 | Quality Level 100 | Quality Level 100 |
| mp 48-53 °C (lit.) | mp 69-73 °C | mp 103-106 °C |
| functional group amine | functional group aldehyde, bromo | functional group aldehyde |
Application
4-Phenylbenzylamine may be used in the synthesis of:
4-Phenylbenzylamine may also be used in the synthesis of Gd3+ chelates of DOTA(1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetate) type ligands.[4]
- squaric acid asymmetric diamides of glycopeptide antibiotics[1]
- asymmetric diamides of daunomycin and carminomycin[2]
- N-(biphenyl-4-ylmethyl)-1-hydroxy-6-thioxo-1,6-dihydropyridine-2-carboxamide[3]
4-Phenylbenzylamine may also be used in the synthesis of Gd3+ chelates of DOTA(1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetate) type ligands.[4]
Other Notes
Handle and store under nitrogen to limit formation of impurities.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
224.6 °F - closed cup
Flash Point(C)
107 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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A new series of glycopeptide antibiotics incorporating a squaric acid moiety.
Sztaricskai F, et al.
The Journal of Antibiotics, 59(9), 564-564 (2006)
chemical society(Great Britain)
Journal of the Chemical Society, Part 1 (1993)
A new class of semisynthetic anthracycline glycoside antibiotics incorporating a squaric acid moiety.
Sztaricskai F, et al.
The Journal of Antibiotics, 58(11), 704-704 (2005)
Thioamide hydroxypyrothiones supersede amide hydroxypyrothiones in potency against anthrax lethal factor.
Agrawal A, et al.
Journal of Medicinal Chemistry, 52(4), 1063-1074 (2009)
Coupling fast water exchange to slow molecular tumbling in Gd3+ chelates: why faster is not always better.
Avedano S, et al.
Inorganic Chemistry, 52(15), 8436-8450 (2013)
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