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(2S,7S)-dimethyl 2,7-N,N-dibenzoylaminooct-4-enedioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 872513-99-0 Structure
  • Basic information

    1. Product Name: (2S,7S)-dimethyl 2,7-N,N-dibenzoylaminooct-4-enedioate
    2. Synonyms: (2S,7S)-dimethyl 2,7-N,N-dibenzoylaminooct-4-enedioate
    3. CAS NO:872513-99-0
    4. Molecular Formula:
    5. Molecular Weight: 438.48
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 872513-99-0.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: (2S,7S)-dimethyl 2,7-N,N-dibenzoylaminooct-4-enedioate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2S,7S)-dimethyl 2,7-N,N-dibenzoylaminooct-4-enedioate(872513-99-0)
    11. EPA Substance Registry System: (2S,7S)-dimethyl 2,7-N,N-dibenzoylaminooct-4-enedioate(872513-99-0)
  • 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: 872513-99-0(Hazardous Substances Data)

872513-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 872513-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,5,1 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 872513-99:
(8*8)+(7*7)+(6*2)+(5*5)+(4*1)+(3*3)+(2*9)+(1*9)=190
190 % 10 = 0
So 872513-99-0 is a valid CAS Registry Number.

872513-99-0Downstream Products

872513-99-0Relevant articles and documents

Methods for the synthesis of dicarba bridges in organic compounds

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Page/Page column 116; 128; 129; 130, (2015/11/17)

The present invention relates to methods for forming dicarba bridges in organic compounds. This involves the use of a pair of complementary metathesisable groups on the organic compound, and subjecting the compound to cross-metathesis under microwave radiation conditions. In an alternative, the compounds contain a turn-inducing group between the pair of cross-metathesisable groups to facilitate the cross-metathesis.

An efficient protocol for the cross-metathesis of sterically demanding olefins

Wang, Zhen J.,Jackson, W. Roy,Robinson, Andrea J.

, p. 3006 - 3009 (2013/07/26)

Cross-metathesis of a wide range of previously unreactive, sterically demanding alkenes can be achieved in fair to excellent yield using a commercially available catalyst by a facile strategy involving reversal of steric preference.

Conotoxin analogues and methods for synthesis of intramolecular dicarba bridge-containing peptides

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Page/Page column 62-63; 16, (2010/11/28)

According to the present invention, there is provided a range of new conotoxin derivatives and methods for synthesizing these analogues and other intramolecular dicarba bridge-containing peptides, including dicarba-disulfide bridge-containing peptides.

Controlled synthesis of (S,S)-2,7-diaminosuberic acid: A method for regioselective construction of dicarba analogues of multicystine-containing peptides

Elaridi, Jomana,Patel, Jim,Jackson, W. Roy,Robinson, Andrea J.

, p. 7538 - 7545 (2007/10/03)

(Chemical Equation Presented) A method to facilitate regioselective formation of multiple dicarba isosteres of cystine is described. A sequence of ruthenium-catalyzed cross metathesis and rhodium-catalyzed hydrogenation of nonproteinaceous allylglycine de

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