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BCR137R

苯并[b]萘并[1,2-d]噻吩

BCR®, certified reference material

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About This Item

经验公式（希尔记法）:
C16H10S
CAS号:
205-43-6
分子量:
234.32
Beilstein:
9635
MDL號碼:
MFCD00215942
分類程式碼代碼:
41116107
PubChem物質ID:
329774226
NACRES:
NA.24

等級

certified reference material

agency

BCR®

製造商／商標名

JRC

技術

HPLC: suitable
gas chromatography (GC): suitable

形式

neat

儲存溫度

2-8°C

SMILES 字串

c1ccc2c(c1)ccc3sc4ccccc4c23

InChI

1S/C16H10S/c1-2-6-12-11(5-1)9-10-15-16(12)13-7-3-4-8-14(13)17-15/h1-10H

InChI 密鑰

XZUMOEVHCZXMTR-UHFFFAOYSA-N

相关类别

分析報告

For more information please see:
BCR137R

法律資訊

BCR is a registered trademark of European Commission

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

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分析证书(COA)

Lot/Batch Number

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Jose Juan Rodríguez et al.
Organic & biomolecular chemistry, 10(36), 7334-7346 (2012-08-01)
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 evaluated. Also, their binding modes have been modelled using docking techniques. It was found that the introduction of
J Jacob et al.
Cancer letters, 32(1), 107-116 (1986-07-01)
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 observed. In case of benzo[b]naphtho[2,3-d]thiophene the formation of a p-quinone takes place. Rat

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