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104770-12-9

(1R,2R,3S,4S)-3-Benzoylamino-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 104770-12-9 Structure

  • Basic information

    1. Product Name: (1R,2R,3S,4S)-3-Benzoylamino-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid ethyl ester
    2. Synonyms:
    3. CAS NO:104770-12-9
    4. Molecular Formula:
    5. Molecular Weight: 285.343
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 104770-12-9.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: (1R,2R,3S,4S)-3-Benzoylamino-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid ethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,2R,3S,4S)-3-Benzoylamino-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid ethyl ester(104770-12-9)
    11. EPA Substance Registry System: (1R,2R,3S,4S)-3-Benzoylamino-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid ethyl ester(104770-12-9)

  • 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: 104770-12-9(Hazardous Substances Data)

104770-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104770-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,7 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104770-12:
(8*1)+(7*0)+(6*4)+(5*7)+(4*7)+(3*0)+(2*1)+(1*2)=99
99 % 10 = 9
So 104770-12-9 is a valid CAS Registry Number.

104770-12-9Relevant articles and documents

Synthesis of novel functionalized cispentacins through C-C oxidative cleavage of diendo-norbornene β-amino acid

Cherepanova, Maria,Kiss, Lorand,Sillanpaeae, Reijo,Fueloep, Ferenc

, p. 9757 - 9763 (2013/09/02)

Difunctionalized cispentacin derivatives with two new stereogenic centres have been synthesized from a diendo-norbornene β-amino acid in a stereocontrolled route, involving C-C double bond functionalization by dihydroxylation, followed by oxidative ring cleavage and transformation of the dialdehyde intermediates through a Wittig reaction.

STEREOCHEMICAL STUDIES 87; SATURATED HETEROCYCLES 82; SYNTHESIS AND STERIC STRUCTURE OF STEREOISOMERIC N-SUBSTITUTED TETRAHYDRO-1,3-OXAZINES FUSED WITH NORBORNANE OR NORBORNENE

Fueloep, Ferenc,Stajer, Geza,Bernath, Gabor,Sohar, Pal

, p. 5159 - 5168 (2007/10/02)

diendo- and diexo-2-Methylamino and 2-benzylamino-3-hydroxymethylbicycloheptanes and the corresponding bicycloheptenes (5a-d, 7a-d) were synthesized from β-amino acid esters containing the norbornane or norbornene skeleton (3a-d).The aminoal

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