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CAS

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54355-51-0

The chemical compound "(3aR)-3a,4,5,6,7,7a-Hexahydro-3aα,7aα-dimethyl-2-phenyl-4β,7β-epoxy-1H-isoindole-1,3(2H)-dione" is a complex organic molecule with a unique structure. It features a hexahydro core, which means it has six hydrogen atoms attached to a carbon backbone. The compound has two methyl groups (CH3) attached to the 3a and 7a positions, indicating that these are alpha (α) positions. It also includes a phenyl group (C6H5) attached to the 2 position, and an epoxy group (C-O-C) bridging the 4 and 7 positions, which are beta (β) positions. The compound is classified as a 1H-isoindole, which is a type of fused bicyclic ring system, and it has a 1,3-dione functional group, indicating the presence of two carbonyl groups (C=O) at the 1 and 3 positions. This molecule is a chiral compound, as indicated by the "3aR" prefix, which specifies the configuration of the 3a position in the molecule.

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  • 54355-51-0 Structure

  • Basic information

    1. Product Name: (3aR)-3a,4,5,6,7,7a-Hexahydro-3aα,7aα-dimethyl-2-phenyl-4β,7β-epoxy-1H-isoindole-1,3(2H)-dione
    2. Synonyms: (3aR)-3a,4,5,6,7,7a-Hexahydro-3aα,7aα-dimethyl-2-phenyl-4β,7β-epoxy-1H-isoindole-1,3(2H)-dione;Cantharidin-N-phenylimide
    3. CAS NO:54355-51-0
    4. Molecular Formula: C16H17NO3
    5. Molecular Weight: 271.31108
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54355-51-0.mol
    9. Article Data: 3

  • 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: (3aR)-3a,4,5,6,7,7a-Hexahydro-3aα,7aα-dimethyl-2-phenyl-4β,7β-epoxy-1H-isoindole-1,3(2H)-dione(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3aR)-3a,4,5,6,7,7a-Hexahydro-3aα,7aα-dimethyl-2-phenyl-4β,7β-epoxy-1H-isoindole-1,3(2H)-dione(54355-51-0)
    11. EPA Substance Registry System: (3aR)-3a,4,5,6,7,7a-Hexahydro-3aα,7aα-dimethyl-2-phenyl-4β,7β-epoxy-1H-isoindole-1,3(2H)-dione(54355-51-0)

  • 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: 54355-51-0(Hazardous Substances Data)

54355-51-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54355-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,5 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54355-51:
(7*5)+(6*4)+(5*3)+(4*5)+(3*5)+(2*5)+(1*1)=120
120 % 10 = 0
So 54355-51-0 is a valid CAS Registry Number.

54355-51-0Downstream Products

54355-51-0Relevant articles and documents

Synthesis of novel N-pyridylcantharidinimides by using high pressure

Lin, Pen-Yuan,Shi, Sheng-Jie,Lin, Lun-Huei,Chen, Hsue-Fen,Hsu, Feng-Lin

, p. 49 - 53 (2001)

The recently described pressure reaction in the presence of trithylamine with subsequent thermal (200°C) cyclization provided 13N-pyridylcantharidinimides 4a-4m from aminopyridines and cantharidin in yields of 15-83%. 2-Amino-3,5-dichloropyridine failed t

Containing chromon structure pyrromonazole Norcantharidin derivative and its preparation method and application

-

Paragraph 0013; 00387, (2017/02/24)

The invention discloses a novel chromone structure-containing pyrazole norcantharidin derivative, and a preparation method and an application thereof. The preparation method comprises the following steps of: introducing a pyrazole ring to the sites C5 and C6 in the norcantharidin structure by a 1,3-dipolar cycloaddition method, and reacting the norcantharidin with the pyrazole ring with chromone derivatives to import the chromone structure to synthesize a series of total 6 novel chromone structure-containing pyrazole norcantharidin derivatives; as a result, the activity of the norcantharidin is improved. The chromone structure-containing pyrazole norcantharidin derivatives provided by the invention are applied to the synthesis of anti-tumor drugs, and have wide application prospect.

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