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C29H35N5O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1338252-04-2 Structure
  • Basic information

    1. Product Name: C29H35N5O2
    2. Synonyms:
    3. CAS NO:1338252-04-2
    4. Molecular Formula:
    5. Molecular Weight: 485.629
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1338252-04-2.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: C29H35N5O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C29H35N5O2(1338252-04-2)
    11. EPA Substance Registry System: C29H35N5O2(1338252-04-2)
  • 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: 1338252-04-2(Hazardous Substances Data)

1338252-04-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1338252-04-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,2,5 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1338252-04:
(9*1)+(8*3)+(7*3)+(6*8)+(5*2)+(4*5)+(3*2)+(2*0)+(1*4)=142
142 % 10 = 2
So 1338252-04-2 is a valid CAS Registry Number.

1338252-04-2Downstream Products

1338252-04-2Relevant articles and documents

Synthesis and biological evaluation of 4-piperidinecarboxylate and 4-piperidinecyanide derivatives for T-type calcium channel blockers

Woo, Hyun Min,Lee, Yun Suk,Roh, Eun Joo,Seo, Seon Hee,Song, Chi Man,Chung, Hye Jin,Pae, Ae Nim,Shin, Kye Jung

, p. 5910 - 5915 (2011/10/09)

To obtain selective and potent inhibitor for T-type calcium channel by ligand based drug design, 4-piperidinecarboxylate and 4-piperidinecyanide derivatives were prepared and evaluated for in vitro and in vivo activity against α1G calcium channel. Among them, several compounds showed good T-type calcium channel inhibitory activity and minimal off-target activity over hERG channel (% inhibition at 10 μM = 61.85-71.99, hERG channel IC50 = 1.57 ± 0.14-4.98 ± 0.36 μM). Selected compound 31a was evaluated on SNL model of neuropathic pain and showed inhibitory effect on mechanical allodynia.

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