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226398-48-7

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226398-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226398-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,3,9 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 226398-48:
(8*2)+(7*2)+(6*6)+(5*3)+(4*9)+(3*8)+(2*4)+(1*8)=157
157 % 10 = 7
So 226398-48-7 is a valid CAS Registry Number.

226398-48-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-[(4-fluorophenyl)sulfanyl]piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names tert-butyl 4-((4-fluorophenyl)thio)piperidine-1-carboxylate

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:226398-48-7 SDS

226398-48-7Relevant articles and documents

TETRAHYDROPYRIDOPYRAZINES MODULATORS OF GPR6

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Paragraph 0160, (2015/07/02)

The present invention provides compounds of formula I: which are useful as modulators of GPR6, pharmaceutical compositions thereof, methods for treatment of conditions associated with GPR6, processes for making the compounds and intermediates thereof.

PYRAZINES MODULATORS OF GPR6

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Paragraph 0141, (2015/09/22)

The present invention provides compounds of formula (I): which are useful as modulators of GPR6, pharmaceutical compositions thereof, methods for treatment of conditions associated with GPR6, processes for making the compounds and intermediates thereof.

Discovery of a piperidine-4-carboxamide CCR5 antagonist (TAK-220) with highly potent anti-HIV-1 activity

Imamura, Shinichi,Ichikawa, Takashi,Nishikawa, Youichi,Kanzaki, Naoyuki,Takashima, Katsunori,Niwa, Shinichi,Iizawa, Yuji,Baba, Masanori,Sugihara, Yoshihiro

, p. 2784 - 2793 (2007/10/03)

We incorporated various polar groups into previously described piperidine-4-carboxamide CCR5 antagonists to improve their metabolic stability in human hepatic microsomes. Introducing a carbamoyl group into the phenyl ring of the 4-benzylpiperidine moiety

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