benzo[b]naphtho[1,2-d]thiophene

Modify Date: 2024-01-08 20:23:51

benzo[b]naphtho[1,2-d]thiophene structure	Common Name	benzo[b]naphtho[1,2-d]thiophene
	CAS Number	205-43-6	Molecular Weight	234.316
	Density	1.3±0.1 g/cm3	Boiling Point	434.3±14.0 °C at 760 mmHg
	Molecular Formula	C₁₆H₁₀S	Melting Point	185℃ (acetic acid )
	MSDS	N/A	Flash Point	163.0±6.3 °C

Name	naphtho[2,1-b][1]benzothiole
Synonym	More Synonyms

Density	1.3±0.1 g/cm3
Boiling Point	434.3±14.0 °C at 760 mmHg
Melting Point	185℃ (acetic acid )
Molecular Formula	C₁₆H₁₀S
Molecular Weight	234.316
Flash Point	163.0±6.3 °C
Exact Mass	234.050323
PSA	28.24000
LogP	5.61
Vapour Pressure	0.0±1.0 mmHg at 25°C
Index of Refraction	1.810
Storage condition	2-8°C

CHEMICAL IDENTIFICATION

RTECS NUMBER :: DI2340000

CHEMICAL NAME :: Benzo(b)naphtho(1,2-d)thiophene

CAS REGISTRY NUMBER :: 205-43-6

BEILSTEIN REFERENCE NO. :: 0009635

LAST UPDATED :: 199612

DATA ITEMS CITED :: 1

MOLECULAR FORMULA :: C16-H10-S

MOLECULAR WEIGHT :: 234.32

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :: Mutation in microorganisms

TEST SYSTEM :: Bacteria - Salmonella typhimurium

DOSE/DURATION :: 40 ug/plate

REFERENCE :: CRTOEC Chemical Research in Toxicology. (American Chemical Soc., Distribution Office Dept. 223, POB 57/36, West End Station, Washington, DC 20037) V.1- 1988- Volume(issue)/page/year: 3,93,1990

RTECS	DI2340000
HS Code	2934999090

Precursor 6
CAS#:1264712-19-7 3-[1-(2-fluorop... CAS#:20841-53-6 naphtho[2,1-b][... CAS#:354816-86-7 2,3,5,6-tetrahy... CAS#:1264712-17-5 1-(2-fluorophen...
CAS#:1993-03-9 2-Fluorophenylb... CAS#:605-02-7 1-PHENYLNAPHTHALENE
DownStream 4
CAS#:605-02-7 1-PHENYLNAPHTHALENE CAS#:3018-20-0 1-phenyl-1,2,3,... CAS#:67064-63-5 5-phenyl-1,2,3,... CAS#:90501-14-7 tetrahydro(1,2,...

HS Code	2934999090
Summary	2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

The predominant role of S-oxidation in rat liver metabolism of thiaarenes.

Cancer Lett. 32(1) , 107-16, (1986)

Thiaarenes are metabolized by liver microsomes of untreated rats predominantly to sulfones and sulfoxides. After pretreatment of rats with monooxygenase inducers, ring oxidation of thiaarenes is also ...

Towards β-selectivity in functional estrogen receptor antagonists.

Org. Biomol. Chem. 10(36) , 7334-46, (2012)

Based on the benzo[b]naphtho[1,2-d]furan and benzo[b]naphtho[1,2-d]thiophene frameworks, a series of ligands with different basic side chains (BSCs) has been synthesized and pharmacologically evaluate...

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