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1383617-02-4

3,5-dimethoxybenzyl-N-succinimidyl carbonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1383617-02-4 Structure

  • Basic information

    1. Product Name: 3,5-dimethoxybenzyl-N-succinimidyl carbonate
    2. Synonyms: 3,5-dimethoxybenzyl-N-succinimidyl carbonate
    3. CAS NO:1383617-02-4
    4. Molecular Formula:
    5. Molecular Weight: 309.276
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1383617-02-4.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: 3,5-dimethoxybenzyl-N-succinimidyl carbonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,5-dimethoxybenzyl-N-succinimidyl carbonate(1383617-02-4)
    11. EPA Substance Registry System: 3,5-dimethoxybenzyl-N-succinimidyl carbonate(1383617-02-4)

  • 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: 1383617-02-4(Hazardous Substances Data)

1383617-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1383617-02-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,6,1 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1383617-02:
(9*1)+(8*3)+(7*8)+(6*3)+(5*6)+(4*1)+(3*7)+(2*0)+(1*2)=164
164 % 10 = 4
So 1383617-02-4 is a valid CAS Registry Number.

1383617-02-4Downstream Products

1383617-02-4Relevant articles and documents

Synthesis and evaluation of novel caged DNA alkylating agents bearing 3,4-epoxypiperidine structure

Kawada, Yuji,Kodama, Tetsuya,Miyashita, Kazuyuki,Imanishi, Takeshi,Obika, Satoshi

experimental part, p. 5102 - 5108 (2012/08/08)

Previously, we reported that the 3,4-epoxypiperidine structure, whose design was based on the active site of DNA alkylating antitumor antibiotics, azinomycins A and B, possesses prominent DNA cleavage activity. In this report, novel caged DNA alkylating agents, which were designed to be activated by UV irradiation, were synthesized by the introduction of four photo-labile protecting groups to a 3,4-epoxypiperidine derivative. The DNA cleavage activity and cytotoxicity of the caged DNA alkylating agents were examined under UV irradiation. Four caged DNA alkylating agents showed various degrees of bioactivity depending on the photosensitivity of the protecting groups.

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