BENZO(B)NAPHTHO(2,1-D)THIOPHENE

Product Name: BENZO(B)NAPHTHO(2,1-D)THIOPHENE
CAS No.: 239-35-0
Chemical Name: BENZO(B)NAPHTHO(2,1-D)THIOPHENE
Synonyms: Zavegepant Impurity 5;11-thiabenzo(a)fluorene;Benzo[a]dibenzothiophene;1,2-Benzo-9-thiafluorene;3,4-Benzodibenzothiophene;Naphtho[1,2-b]thianaphthene;BENZO(B)NAPH(2,1-D)THIOPHENE;BENZONAPHTHO(2,1-D)THIOPHENE;1,2-BENZODIPHENYLENE SULFIDE;BENZO[B]NAPHTHO[2,1-D]THIOPH
CBNumber: CB4716233
Molecular Formula: C16H10S
Formula Weight: 234.32
MOL File: 239-35-0.mol

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BENZO(B)NAPHTHO(2,1-D)THIOPHENE Property

Melting point:: 188-190 °C (lit.)
Boiling point:: 434.3±14.0 °C(Predicted)
Density: 1.292±0.06 g/cm3(Predicted)
solubility: chloroform: soluble2.5%, clear to very slightly hazy, colorless to faint yellow or tan
IARC: 3 (Vol. 103) 2013
EPA Substance Registry System: Benzo[b]naphtho[2,1-d]thiophene (239-35-0)

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Safety

WGK Germany: 3

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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 255122
Product name: 1,2-Benzodiphenylene sulfide
Purity: 99%
Packaging: 25mg
Price: $101
Updated: 2023/06/20

TRC

Product number: B207085
Product name: 1,2-Benzo-9-thiafluorene
Packaging: 5mg
Price: $95
Updated: 2021/12/16

AK Scientific

Product number: 1391AQ
Product name: 1,2-Benzodiphenylene sulfide
Packaging: 25mg
Price: $160
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: CHM0005721
Product name: 1,2-BENZODIPHENYLENE SULPHIDE
Purity: 95.00%
Packaging: 25MG
Price: $619.47
Updated: 2021/12/16

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BENZO(B)NAPHTHO(2,1-D)THIOPHENE Chemical Properties,Usage,Production

Uses

1,2-Benzodiphenylene sulfide has been used in direct screening of sediment samples for polycyclic aromatic hydrocarbons by flow manifold coupled on-line to a fluorimetric detector.

Definition

ChEBI: Benzo[b]naphtho[2,1-d]thiophene is an organosulfur heterocyclic compound and an organic heterotricyclic compound.

General Description

1,2-benzodiphenylene sulfide is a rare constituent of coal tar. Photodeoxygenation of 1,2-benzodiphenylene sulfoxide, generates an intermediate capable of oxidizing the solvent benzene to phenol. Liquid-phase photolysis of 1,2-benzodiphenylene sulfide to generate atomic oxygen [O(³P)] or an equivalent active oxygen species has been reported.

BENZO(B)NAPHTHO(2,1-D)THIOPHENE Preparation Products And Raw materials

Raw materials

Preparation Products

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BENZO(B)NAPHTHO(2,1-D)THIOPHENE Suppliers

China 26 Germany 2 India 1 Norway 1 Switzerland 1 United Kingdom 3 United States 5 Global 39

Syntechem Co.,Ltd

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Sigma-Aldrich

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Yurui (Shanghai) Chemical Co., Ltd.

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239-35-0, BENZO(B)NAPHTHO(2,1-D)THIOPHENERelated Search:

Etomidate Thianaphthene Dibenzothiophene BENZO(B)NAPHTHO(2,3-D)THIOPHENE,30578, Benzo[b]naphtho[2,3-d]thiophene ( purity),Benzo[b]naphtho[2,3-d]thiophene, 99.5+% DETOMIDINE HYDROCHLORIDE Detomidine hydrochloride BENZO(B)NAPHTHO(2,1-B)THIOPHENE Benzo[b]naphtho[1,2-d]thiophene (purity),39696, Benzo[b]naphtho[1,2-d]thiophene ( purity),BENZO(B)NAPHTHO(1,2-D)THIOPHENE 4-(2,3-DIMETHYL-BENZYL)-1H-IMIDAZOLE BENZO(B)NAPHTHO(2,1-D)THIOPHENE SPECS AM-944/40947649 DIPHENANTHRO[9,10-B:9',10'-D]THIOPHENE THIOPHENE-D4 DIBENZO[2,3:10,11]PERYLENO[1,12-BCD]THIOPHENE

1,2-BENZODIPHENYLENE SULFIDE

1,2-BENZODIPHENYLENE SULPHIDE

BENZO(B)NAPHTHO(2,1-D)THIOPHENE

1,2-Benzo-9-thiafluorene

Benzo[a]dibenzothiophene

Benzo[b]naphtho[2,1]thiophene

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

Naphtho[1,2-b][1]benzothiophene

Naphtho[1,2-b]thianaphthene

BENZONAPHTHO(2,1-D)THIOPHENE

BENZO(B)NAPH(2,1-D)THIOPHENE

BENZO[B]NAPHTHO[2,1-D]THIOPH

1,2-BENZODIPHENYLENE SULPHIDE 99%

3,4-(1,3-Butadiene-1,4-diyl)dibenzothiophene

3,4-[1,3]Butadienodibenzothiophene

3,4-Benzodibenzothiophene

naphtho[1,2-b][1]benzothiole

naphtho[1,2-b]benzothiophene

11-thiabenzo(a)fluorene

naphtho(1,2:2,3)thionaphthen

1,2-Benzodiphenylene sulfide,Benzo[b]naphtho[2,1-d]thiophene

1,2-Benzodiphenylene sulfide 99%

Zavegepant Impurity 5

Benzo[b]naphtho[2,1-d]thiophene in toluene

C20600000 Benzo[b]naphtho[2,1-d]thiophene

L20600000CY Benzo[b]naphtho[2,1-d]thiophenE10

239-35-0

Heterocyclic Building Blocks

Others

S-Containing

Building Blocks

Heterocyclic Compounds