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4-PYRIMIDIN-2-YL-PIPERAZINE-1-CARBONYL CHLORIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 253176-26-0 Structure
  • Basic information

    1. Product Name: 4-PYRIMIDIN-2-YL-PIPERAZINE-1-CARBONYL CHLORIDE
    2. Synonyms: 4-PYRIMIDIN-2-YL-PIPERAZINE-1-CARBONYL CHLORIDE
    3. CAS NO:253176-26-0
    4. Molecular Formula: C9H11ClN4O
    5. Molecular Weight: 226.66
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 253176-26-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-PYRIMIDIN-2-YL-PIPERAZINE-1-CARBONYL CHLORIDE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-PYRIMIDIN-2-YL-PIPERAZINE-1-CARBONYL CHLORIDE(253176-26-0)
    11. EPA Substance Registry System: 4-PYRIMIDIN-2-YL-PIPERAZINE-1-CARBONYL CHLORIDE(253176-26-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 253176-26-0(Hazardous Substances Data)

253176-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 253176-26-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,1,7 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 253176-26:
(8*2)+(7*5)+(6*3)+(5*1)+(4*7)+(3*6)+(2*2)+(1*6)=130
130 % 10 = 0
So 253176-26-0 is a valid CAS Registry Number.

253176-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-pyrimidin-2-ylpiperazine-1-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 4-PYRIMIDIN-2-YL-PIPERAZINE-1-CARBONYL CHLORIDE

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:253176-26-0 SDS

253176-26-0Downstream Products

253176-26-0Relevant articles and documents

Design, synthesis and anti-inflammatory effects of novel 9-O-substituted-berberine derivatives

Huang, Mei-Yan,Lin, Jing,Huang, Zhi-Jian,Xu, Hong-Gui,Hong, Juan,Sun, Ping-Hua,Guo, Jia-Liang,Chen, Wei-Min

, p. 658 - 666 (2016/05/19)

Berberine, an isoquinoline alkaloid in many medicinal herbs, has been found to possess broad pharmacological activities. A series of novel C-9-O-substituted-berberine derivatives have been synthesized and their anti-inflammatory effects evaluated both in vitro and in vivo. Compared to berberine, the new synthetic berberine derivatives 3i and 5e exhibit significantly improved inhibitory activities against the release of NO, TNF-α and IL-6. Furthermore, derivatives 3i and 5e were found to inhibit more effectively the migration of neutrophils and primitive macrophage in transgenic zebrafish larvae with injury-provoked inflammation. Pre-treatment with derivatives 3i or 5e could lead to a concentration-dependent decrease in nuclear factor-κB (NF-κB) p65 and NF-κB inhibitor α (IκBα) phosphorylation and inducible nitric oxide synthase (iNOS) expression in lipopolysaccharide (LPS)-induced RAW264.7 cells, which suggested that the anti-inflammatory activities of berberine derivatives 3i and 5e are related to their suppression of the NF-κB signal pathway.

Beta lactam compounds and their use as inhibitors of tryptase

-

Page column 123, (2010/11/29)

Compounds of the formulas: are disclosed. These compounds inhibit tryptase as well as other enzyme systems or are selective tryptase inhibitors and are useful as antiinflammatory agents particularly in the treatment of chronic asthma.

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