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Merck
모든 사진(1)

문서

B27005

Sigma-Aldrich

3-Benzyloxybenzaldehyde

98%

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About This Item

Linear Formula:
C6H5CH2OC6H4CHO
CAS Number:
Molecular Weight:
212.24
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

98%

형태

chunks

mp

56-58 °C (lit.)

SMILES string

O=Cc1cccc(OCc2ccccc2)c1

InChI

1S/C14H12O2/c15-10-13-7-4-8-14(9-13)16-11-12-5-2-1-3-6-12/h1-10H,11H2

InChI key

JAICGBJIBWDEIZ-UHFFFAOYSA-N

애플리케이션

Some of the reported applications of 3-benzyloxybenzaldehyde are:
  • Synthesis of silybin analogs as anticancer agents that produce apoptosis in ovarian cancer cells through tubulin inhibition.
  • Synthesis of porphyrin and boron dipyrromethene (BODIPY) derivatives for fluorescent applications.
  • Preparation of styrene copolymers with varying chain mobilities.
  • Synthesis of aromatic derivatives of trimethoprim as potential antimalarial agents.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


시험 성적서(COA)

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Synthesis of a novel BODIPY library and its application in the discovery of a fructose sensor.
Zhai D, et al.
ACS Combinatorial Science, 14(2), 81-84 (2012)
Design and discovery of silybin analogues as antiproliferative compounds using a ring disjunctive?Based, natural product lead optimization approach.
Manivannan E, et al.
European Journal of Medicinal Chemistry, 133, 365-378 (2017)
Novel Copolymers of Styrene. 2. Oxy Ring-Substituted 2-Cyano-3-phenyl 2-propenamides.
Kharas G B, et al.
Journal of Macromolecular Science, Part A: Pure and Applied Chemistry, 50(8), 797-802 (2013)
Synthesis of Functionalized trans?A2B2?Porphyrins Using Donor?Acceptor Cyclopropane?Derived Dipyrromethanes.
Beyzavi M H, et al.
Advanced Synthesis & Catalysis, 355(7), 1409-1422 (2013)
Target guided synthesis of 5-benzyl-2, 4-diamonopyrimidines: their antimalarial activities and binding affinities to wild type and mutant dihydrofolate reductases from Plasmodium falciparum.
Sirichaiwat C, et al.
Journal of Medicinal Chemistry, 47(2), 345-354 (2004)

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