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Merck
모든 사진(1)

주요 문서

552313

Sigma-Aldrich

4-Phenylbenzylamine

97%

동의어(들):

(4-Phenylphenyl)methanamine, 1-(Biphenyl-4-yl)methanamine, 4-(Aminomethyl)biphenyl, 4-Biphenylmethylamine, Biphenyl-4-ylmethanamine, [(1,1′-Biphenyl-4-yl)methyl]amine, [(Biphenyl-4-yl)methyl]amine, [1,1′-Biphenyl]-4-ylmethanamine, p-Phenylbenzylamine

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About This Item

Linear Formula:
C6H5C6H4CH2NH2
CAS Number:
Molecular Weight:
183.25
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

97%

mp

48-53 °C (lit.)

작용기

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

애플리케이션

4-Phenylbenzylamine may be used in the synthesis of:
  • squaric acid asymmetric diamides of glycopeptide antibiotics
  • asymmetric diamides of daunomycin and carminomycin
  • N-(biphenyl-4-ylmethyl)-1-hydroxy-6-thioxo-1,6-dihydropyridine-2-carboxamide

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.

기타 정보

Handle and store under nitrogen to limit formation of impurities.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

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

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

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)
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)
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)
Thioamide hydroxypyrothiones supersede amide hydroxypyrothiones in potency against anthrax lethal factor.
Agrawal A, et al.
Journal of Medicinal Chemistry, 52(4), 1063-1074 (2009)

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