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A45807

Sigma-Aldrich

2-Amino-5-chlorobenzoxazole

97%

Synonym(s):

Zoxazolamine

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About This Item

Empirical Formula (Hill Notation):
C7H5ClN2O
CAS Number:
61-80-3
Molecular Weight:
168.58
EC Number:
200-519-4
MDL number:
MFCD00005770
UNSPSC Code:
12352100
PubChem Substance ID:
24890884
NACRES:
NA.22

Assay

97%

form

powder

mp

181-184 °C (lit.)

SMILES string

Nc1nc2cc(Cl)ccc2o1

InChI

1S/C7H5ClN2O/c8-4-1-2-6-5(3-4)10-7(9)11-6/h1-3H,(H2,9,10)

InChI key

YGCODSQDUUUKIV-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Magnolol has been reported to strongly inhibit the mutagenicity induced by indirect mutagens in the Ames test as well as the clastogenicity induced by benzo(a)pyrene (B(a)P) in the mice micronucleus test. Here, we evaluated the inhibitory effect of magnolol on
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European journal of drug metabolism and pharmacokinetics, 28(1), 7-10 (2003-09-25)
The influence of four ethanolamine derivatives with anti-inflammatory and antioxidant activity on the in vitro aminopyrine N-demethylation was studied. It was found that these compounds inhibit the N-demethylation of aminopyrine. 1-Cyclohexyl-5-(2-hydroxy-ethylamino)-pentan-2-one (compound 4), possessing the highest inhibitory activity and found
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The Indian journal of medical research, 135, 211-216 (2012-03-27)
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