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CAS

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460748-94-1

(4S,5S)-2,2-Dimethyl-[1,3]dioxolane-4,5-dicarboxylic acid bis-[(2-hydroxy-5-nitro-phenyl)-amide] is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 460748-94-1 Structure

  • Basic information

    1. Product Name: (4S,5S)-2,2-Dimethyl-[1,3]dioxolane-4,5-dicarboxylic acid bis-[(2-hydroxy-5-nitro-phenyl)-amide]
    2. Synonyms:
    3. CAS NO:460748-94-1
    4. Molecular Formula:
    5. Molecular Weight: 462.373
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 460748-94-1.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: (4S,5S)-2,2-Dimethyl-[1,3]dioxolane-4,5-dicarboxylic acid bis-[(2-hydroxy-5-nitro-phenyl)-amide](CAS DataBase Reference)
    10. NIST Chemistry Reference: (4S,5S)-2,2-Dimethyl-[1,3]dioxolane-4,5-dicarboxylic acid bis-[(2-hydroxy-5-nitro-phenyl)-amide](460748-94-1)
    11. EPA Substance Registry System: (4S,5S)-2,2-Dimethyl-[1,3]dioxolane-4,5-dicarboxylic acid bis-[(2-hydroxy-5-nitro-phenyl)-amide](460748-94-1)

  • 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: 460748-94-1(Hazardous Substances Data)

460748-94-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 460748-94-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,0,7,4 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 460748-94:
(8*4)+(7*6)+(6*0)+(5*7)+(4*4)+(3*8)+(2*9)+(1*4)=171
171 % 10 = 1
So 460748-94-1 is a valid CAS Registry Number.

460748-94-1Downstream Products

460748-94-1Relevant articles and documents

Synthesis of novel C2-symmetric and enantiomerically pure bisbenzoxazoles and bisbenzothiazoles derived from L- and D-tartaric acids

Jiao, Peng,Xu, Jiaxi,Zhang, Qihan,Choi, Michael C.K.,Chan, Albert S.C.

, p. 3081 - 3088 (2001)

Five pairs of novel C2-symmetric and enantiomerically pure bisbenzoxazoles and a pair of bisbenzothiazoles derived from L- and D-tartaric acids have been synthesized from L- and D-2,3-O-isopropylidenetartaric dichlorides and o-aminophenol derivatives or o-aminothiophenol, respectively, in two- or one-step reactions. The mechanism for the formation of bisbenzoxazoles and bisbenzothiazoles was suggested. The UV and 1H NMR spectra showed that no coordination between the bisbenzoheterazoles and Cu(I) or Ni(II) cations occurred due to the lack of a sufficiently basic nitrogen donor atom in the benzoheterazole moiety.

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