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158985-36-5

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158985-36-5 Usage

General Description

1-Boc-4-(4-methoxycarbonylphenyl)piperazine is a chemical compound with the molecular formula C18H26N2O4. It is a derivative of piperazine and contains a 4-(4-methoxycarbonylphenyl) moiety attached to the piperazine ring. The compound has a tert-butoxycarbonyl (Boc) protecting group on the nitrogen atom of the piperazine ring. 1-Boc-4-(4-methoxycarbonylphenyl)piperazine is used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It may also have potential applications in medicinal chemistry and drug development due to its structural features and pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 158985-36-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,9,8 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 158985-36:
(8*1)+(7*5)+(6*8)+(5*9)+(4*8)+(3*5)+(2*3)+(1*6)=195
195 % 10 = 5
So 158985-36-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H24N2O4/c1-17(2,3)23-16(21)19-11-9-18(10-12-19)14-7-5-13(6-8-14)15(20)22-4/h5-8H,9-12H2,1-4H3

158985-36-5 Well-known Company Product Price

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  • Aldrich

  • (652385)  1-Boc-4-(4-methoxycarbonylphenyl)piperazine  97%

  • 158985-36-5

  • 652385-1G

  • 1,258.92CNY

  • Detail
  • Aldrich

  • (652385)  1-Boc-4-(4-methoxycarbonylphenyl)piperazine  97%

  • 158985-36-5

  • 652385-5G

  • 4,132.44CNY

  • Detail

158985-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl 4-(4-methoxycarbonylphenyl)piperazine-1-carboxylate

1.2 Other means of identification

Product number -
Other names 4-(4-N-Boc-piperazinyl)benzylalcohol

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:158985-36-5 SDS

158985-36-5Relevant articles and documents

ROR [gamma]t inhibitor, preparation method and application thereof

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Paragraph 1342; 1344-1346, (2021/07/08)

The invention relates to the technical field of medicines, in particular to an ROR [gamma]t inhibitor, a preparation method and application thereof. The invention also relates to a pharmaceutical composition containing the compound, a method for preparing the pharmaceutical composition, and application of the compound or the pharmaceutical composition in treatment or prevention of ROR [gamma]t-mediated cancers, inflammations or autoimmune diseases of mammals, especially human beings.

PYRAZOLOTRIAZOLOPYRIMIDINE DERIVATIVES AS A2A RECEPTOR ANTAGONIST

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Paragraph 0653-0655, (2020/02/16)

Disclosed herein is a pyrazolotriazolopyrimidine derivative or a stereoisomer thereof, or a pharmaceutically acceptable salt thereof useful as A2A receptor antagonist, and a pharmaceutical composition comprising the same. Also disclosed herein is a method of treating cancer using the pyrazolotriazolopyrimidine derivative or a stereoisomer thereof, or a pharmaceutically acceptable salt thereof as A2A receptor antagonist.

CEREBLON LIGANDS AND BIFUNCTIONAL COMPOUNDS COMPRISING THE SAME

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Paragraph 1010; 1011; 1012, (2018/08/20)

The description relates to cereblon E3 ligase binding compounds, including bifunctional compounds comprising the same, which find utility as modulators of targeted ubiquitination, especially inhibitors of a variety of polypeptides and other proteins which are degraded and/or otherwise inhibited by bifunctional compounds according to the present disclosure. In particular, the description provides compounds, which contain on one end a ligand which binds to the cereblon E3 ubiquitin ligase and on the other end a moiety which binds a target protein such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of that protein. Compounds can be synthesized that exhibit a broad range of pharmacological activities consistent with the degradation/inhibition of targeted polypeptides of nearly any type.

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