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131454-98-3

2-endo-Acetamido-2-exo-phenylaminonorbornene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 131454-98-3 Structure

  • Basic information

    1. Product Name: 2-endo-Acetamido-2-exo-phenylaminonorbornene
    2. Synonyms:
    3. CAS NO:131454-98-3
    4. Molecular Formula:
    5. Molecular Weight: 242.321
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131454-98-3.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: 2-endo-Acetamido-2-exo-phenylaminonorbornene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-endo-Acetamido-2-exo-phenylaminonorbornene(131454-98-3)
    11. EPA Substance Registry System: 2-endo-Acetamido-2-exo-phenylaminonorbornene(131454-98-3)

  • 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: 131454-98-3(Hazardous Substances Data)

131454-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131454-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,4,5 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 131454-98:
(8*1)+(7*3)+(6*1)+(5*4)+(4*5)+(3*4)+(2*9)+(1*8)=113
113 % 10 = 3
So 131454-98-3 is a valid CAS Registry Number.

131454-98-3Downstream Products

131454-98-3Relevant articles and documents

A two-step synthesis of 2-exo-substituted 2-endo-aminonorbornenes from 2-acetamidonorbornene-2-carboxylic acids

Yamazaki,Horikawa,Nishitani,Iwasaki,Okamura,Date

, p. 541 - 548 (1991)

2-exo-Substituted 2-endo-acetamidonorbornenes (3) were synthesized in a two-step procedure from 2-acetamidonorbornene-2-carboxylic acids (1, 1') with exceedingly high exo-selectivities based on a new approach involving anodic decarboxylation followed by o

A SYNTHESIS OF 2-EXO-SUBSTITUTED 2-ENDO-AMINONORBORNENES: ORGANOALUMINUM-PROMOTED NUCLEOPHILIC SUBSTITUTION ON 2-ENDO-ACETAMIDO-2-EXO-METHOXYNORBORNENE

Yamazaki, Hiroyoshi,Horikawa, Hiroshi,Nishitani, Takashi,Iwasaki, Tameo

, p. 5345 - 5346 (2007/10/02)

A variety of 2-exo-substituted 2-endo-acetamidonorbornenes (2a-g) were synthesized in exceedingly high exo selectivities by organoaluminum-promoted nucleophilic substitution on 2-endo-acetamido-2-exo-methoxynorbornene.

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