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3601-88-5

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3601-88-5 Usage

Type of compound

Organic heterocyclic

Structural components

Pyrimidine ring, piperazine moiety

Pharmaceutical properties

Potential use in drug development

Target disorders

Psychiatric disorders (e.g., depression, anxiety)

Mechanism of action

Serotonin receptor antagonist

Research areas

Neurodegenerative diseases, cancer therapy

Therapeutic potential

Inhibition of DNA synthesis, cell growth

Versatility

Diverse applications in pharmaceuticals and medical research

Check Digit Verification of cas no

The CAS Registry Mumber 3601-88-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,0 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3601-88:
(6*3)+(5*6)+(4*0)+(3*1)+(2*8)+(1*8)=75
75 % 10 = 5
So 3601-88-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H18N4O/c1-20-14-6-3-2-5-13(14)18-9-11-19(12-10-18)15-16-7-4-8-17-15/h2-8H,9-12H2,1H3

3601-88-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[4-(2-methoxyphenyl)piperazin-1-yl]pyrimidine

1.2 Other means of identification

Product number -
Other names -

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:3601-88-5 SDS

3601-88-5Downstream Products

3601-88-5Relevant articles and documents

HFIP Promoted Low-Temperature SNAr of Chloroheteroarenes Using Thiols and Amines

Bhujabal, Yuvraj B.,Vadagaonkar, Kamlesh S.,Gholap, Aniket,Sanghvi, Yogesh S.,Dandela, Rambabu,Kapdi, Anant R.

, p. 15343 - 15354 (2019/12/04)

A highly efficient and an unprecedented hexafluoro-2-propanol, promoting low-temperature aromatic nucleophilic substitutions of chloroheteroarenes, has been performed using thiols and (secondary) amines under base-free and metal-free conditions. The developed protocol also provides excellent regio-control for the selective functionalization of dichloroheteroarenes, while the utility of the protocol was demonstrated by the modification of a commercially available drug ceritinib.

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