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Merck
CN

162590

2-氨基-6-甲氧基苯并噻唑

98%

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关于此项目

经验公式(希尔记法):
C8H8N2OS
化学文摘社编号:
分子量:
180.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
217-130-0
MDL number:
Assay:
98%
Form:
solid
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assay

98%

form

solid

mp

165-167 °C (lit.)

SMILES string

COc1ccc2nc(N)sc2c1

InChI

1S/C8H8N2OS/c1-11-5-2-3-6-7(4-5)12-8(9)10-6/h2-4H,1H3,(H2,9,10)

InChI key

KZHGPDSVHSDCMX-UHFFFAOYSA-N

General description

2-Amino-6-methoxybenzothiazole undergoes Sandmeyer reaction on heating with isoamyl nitrite and CuBr2 to yield 2-bromo-6-methoxybenzothiazole.

Application

2-Amino-6-methoxybenzothiazole was used as building block in the syntheses of novel series of Schiff bases and 4-thiazolidinones. It was used in the synthesis of 2-cyano-6-methoxybenzothiazole, key intermediate for the synthesis of firefly luciferin.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A Convenient Synthetic Method of 2-Cyano-6-methoxybenzothiazole,-A Key Intermediate for the Synthesis of Firefly Luciferin.
Toya Y, et al.
Bulletin of the Chemical Society of Japan, 65(2), 392-395 (1992)
An efficient palladium catalyzed synthesis of 2-arylbenzothiazoles.
Majo VJ, et al.
Tetrahedron Letters, 44(47), 8535-8537 (2003)
Navin B Patel et al.
Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society, 18(3), 129-136 (2010-07-01)
A novel series of Schiff bases 5a-j and 4-thiazolidinones 6a-j have been prepared from the building blocks 2-chloro pyridine-3-carboxylic acid [1] and 2-amino-6-methoxy-benzothiazole [2]. All of the synthesized compounds have been confirmed by elemental analyses, IR, (1)H NMR and (13)C



全球贸易项目编号

货号GTIN
162590-250G04061832993225
162590-50G04061832993232