260975

Sigma-Aldrich

4-Bromocinnamic acid, predominantly trans

98%

Linear Formula:
BrC6H4CH=CHCO2H
CAS Number:
Molecular Weight:
227.05
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

mp

262-264 °C (lit.)

SMILES string

OC(=O)\C=C\c1ccc(Br)cc1

InChI

1S/C9H7BrO2/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-6H,(H,11,12)/b6-3+

InChI key

CPDDDTNAMBSPRN-ZZXKWVIFSA-N

Related Categories

Application

4-Bromocinnamic acid (trans-4-bromocinnamic acid) has been used in the preparation of:
  • (E)-β-bromo-4-bromostyrene
  • 2-amino-7-(piperidin-4-yl)isoquinoline
  • brominated dansyl derivative (4-bromophenyl)-4-(5-(dimethylamino)naphthalene-1-sulfonamido)butanoic acid

Packaging

5 g in glass bottle
25 g in poly bottle

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Target Organs

Respiratory system

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

NONH for all modes of transport

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis

Certificate of Origin

Design, synthesis, and biological evaluation of a dansyled amino acid derivative as an imaging agent for apoptosis.
Zeng W, et al.
Tetrahedron Letters, 49(45), 6429-6432 (2008)
A Convenient Synthesis of 1-Amino-7-(Piperidin-4-yl) Isoquinoline.
Shkavrov S, et al.
Synthetic Communications, 35(5), 725-730 (2005)
Stereoselective synthesis of (E)-?-arylvinyl bromides by microwave-induced reaction of anti-3-aryl-2, 3-dibromopropanoic acids using an AgOAc-AcOH system.
Kuang C, et al.
Tetrahedron, 61(3), 637-642 (2005)

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