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7441-55-6

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7441-55-6 Usage

Chemical class

Thiosemicarbazides

Molar mass

262.32 g/mol

Structural features

1-[4-(Acetylamino)phenyl]-2-(ethylidene)thiosemicarbazide group

Potential applications

Pharmaceuticals
Biochemistry
Organic synthesis

Structural significance

Thiosemicarbazide structural features

Role in synthesis

Building block for more complex organic compounds

Biological activities

May exhibit interesting biological activities (further research needed)

Research status

Further research needed to fully understand properties and potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 7441-55-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,4 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7441-55:
(6*7)+(5*4)+(4*4)+(3*1)+(2*5)+(1*5)=96
96 % 10 = 6
So 7441-55-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N4OS/c1-7(14-15-11(12)17)9-3-5-10(6-4-9)13-8(2)16/h3-6H,1-2H3,(H,13,16)(H3,12,15,17)/b14-7+

7441-55-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4'-acetamidoacetophenone thiosemicarbazone

1.2 Other means of identification

Product number -
Other names Essigsaeure-[4-(1-thiosemicarbazono-aethyl)-anilid]

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:7441-55-6 SDS

7441-55-6Downstream Products

7441-55-6Relevant articles and documents

Amino-ethanone thiosemicarbazone derivatives and its application

-

Paragraph 0024; 0026, (2016/12/01)

The invention discloses an aminoacetophenone thiosemicarbazone derivative shown as a formula I and application thereof. In the formula I, an amino group connected with R is at 3 position or 4 position of the phenyl ring, and R is selected from C1-C6 alky or halogenated alkyl or alkoxy, aryl or substituted aryl. The related compounds are novel in structure and simple to prepare, are strong in inhibition activity on tyrosinase and have extremely obvious application prospect.

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