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658103

Sigma-Aldrich

5-Thiazolecarboxaldehyde

95%

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About This Item

Empirical Formula (Hill Notation):
C4H3NOS
CAS Number:
1003-32-3
Molecular Weight:
113.14
MDL number:
MFCD02179516
UNSPSC Code:
12352100
PubChem Substance ID:
24884332
NACRES:
NA.22

Quality Level

100

Assay

95%

form

solid

refractive index

n20/D 1.5874

bp

92-94 °C/16 mmHg

density

1.304 g/mL at 25 °C

functional group

aldehyde

SMILES string

O=Cc1cncs1

InChI

1S/C4H3NOS/c6-2-4-1-5-3-7-4/h1-3H

InChI key

ZXRLWHGLEJGMNO-UHFFFAOYSA-N

Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H317,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

208.4 °F - closed cup

Flash Point(C)

98 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCJ7508
MKBG2355V
MKBF4927V
MKBD2544
MKAA1131

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Raju Khatri et al.
Journal of pharmaceutical sciences, 110(1), 412-421 (2020-09-16)
Pregnancy-related hormones (PRH) have emerged as key regulators of hepatic cytochrome P450 (CYP) enzyme expression and function. The impact of PRH on protein levels of CYP3A4 and other key CYP enzymes, and the metabolism of nifedipine (a CYP3A4 substrate commonly
Asmita Pant et al.
Toxicology and applied pharmacology, 365, 61-70 (2019-01-07)
Non-alcoholic fatty liver disease is manifested by hepatic accumulation of triglycerides (TG) and is commonly associated with metabolic syndrome. The isoprenoid farnesol (FOH) modulates lipid metabolism and reduces hepatic TG content in rodents. This effect involves activation of at least
Yiqiang Xie et al.
Pakistan journal of pharmaceutical sciences, 31(5(Special)), 2315-2321 (2018-11-23)
Feng-Liao-Chang-Wei-Kang (FLCWK), a traditional Chinese patent medicine, consists primarily of Polygonum hydropiper and Daphniphyllum calycinum roots. As a complex containing several kinds of flavonoids, FLCWK has the potential to impact the drug metabolism enzyme P450 3A4 (CYP3A4) and nuclear receptors.

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