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1037510-76-1

methyl 7-azidoheptanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1037510-76-1 Structure

  • Basic information

    1. Product Name: methyl 7-azidoheptanoate
    2. Synonyms: methyl 7-azidoheptanoate
    3. CAS NO:1037510-76-1
    4. Molecular Formula:
    5. Molecular Weight: 185.226
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1037510-76-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: methyl 7-azidoheptanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 7-azidoheptanoate(1037510-76-1)
    11. EPA Substance Registry System: methyl 7-azidoheptanoate(1037510-76-1)

  • 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: 1037510-76-1(Hazardous Substances Data)

1037510-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1037510-76-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,7,5,1 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1037510-76:
(9*1)+(8*0)+(7*3)+(6*7)+(5*5)+(4*1)+(3*0)+(2*7)+(1*6)=121
121 % 10 = 1
So 1037510-76-1 is a valid CAS Registry Number.

1037510-76-1Upstream product

1037510-76-1Relevant articles and documents

Discovery of Novel Indoleamine 2,3-Dioxygenase 1 (IDO1) and Histone Deacetylase (HDAC) Dual Inhibitors

Fang, Kun,Dong, Guoqiang,Li, Yu,He, Shipeng,Wu, Ying,Wu, Shanchao,Wang, Wei,Sheng, Chunquan

, p. 312 - 317 (2018)

In order to take advantage of both immunotherapeutic and epigenetic antitumor agents, the first generation of dual indoleamine 2,3-dioxygenase 1 (IDO1) and histone deacetylase (HDAC) inhibitors were designed. The highly active dual inhibitor 10 showed exc

A novel potent nicotinamide phosphoribosyltransferase inhibitor synthesized via click chemistry

Colombano, Giampiero,Travelli, Cristina,Galli, Ubaldina,Caldarelli, Antonio,Chini, Maria Giovanna,Canonico, Pier Luigi,Sorba, Giovanni,Bifulco, Giuseppe,Tron, Gian Cesare,Genazzani, Armando A.

supporting information; experimental part, p. 616 - 623 (2010/07/06)

The inhibition of NAD synthesis or salvage pathways has been proposed as a novel target for antitumoral drugs. Two molecules with this mechanism of action are at present undergoing clinical trials. In searching for similar novel molecules, we exploited co

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