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169058-47-3

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169058-47-3 Usage

Derivative

hydrazide of benzothiazine carboxylic acid

Substituent

methyl group at the 3-position

Applications

pharmaceutical industry, drug development, synthesis of organic molecules

Safety

handle with caution, may have specific safety and handling requirements due to reactivity and toxicity

Check Digit Verification of cas no

The CAS Registry Mumber 169058-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,0,5 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 169058-47:
(8*1)+(7*6)+(6*9)+(5*0)+(4*5)+(3*8)+(2*4)+(1*7)=163
163 % 10 = 3
So 169058-47-3 is a valid CAS Registry Number.

169058-47-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-4H-1,4-benzothiazine-2-carbohydrazide

1.2 Other means of identification

Product number -
Other names HMS1530C17

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:169058-47-3 SDS

169058-47-3Relevant articles and documents

A facile and green synthesis of "5-(3-methyl-7-substituted-4H-1, 4-benzothiazin-2-yl)-4-aryl-4H-1, 2, 4-triazole-3-thiols" under ultrasound irradiation

Khairnar, Bhikan J.,Girase, Pravin S.,Chaudhari

, p. 285 - 289 (2013/06/27)

A series of novel 3-methyl-7-substituted-4H-1, 4-benzothiazine-2- carbohydrazide & corresponding thiosemicarbazide have been synthesized. The 1, 4-benzothiazine thiosemicarbazides i.e. 2-[(3-methyl-7-substituted-4H-1, 4-benzothiazin-2-yl) carbonyl]-N-aryl-hydrazine carbothiamide when cyclised with 2N sodium hydroxide via intramolecular dehydrative cyclisation gave benzothiazonyl triazoles. The given procedure is in 4-steps. The final step is an intramolecular cyclisation is achieved by ultrasound irradiation & also by conventional method. In general, substantial improvement in rates and increase in modest yields observed when reactions are carried out under sonication, compared with classical heating method. The structures of these compounds have been elucidated by spectral (IR, 1H NMR) analysis.

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