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1-Pyrrolidinecarboxylic acid, 3-azido-4-methoxy-, 1,1-dimethylethyl ester, (3S,4S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 372482-13-8 Structure
  • Basic information

    1. Product Name: 1-Pyrrolidinecarboxylic acid, 3-azido-4-methoxy-, 1,1-dimethylethyl ester, (3S,4S)-
    2. Synonyms:
    3. CAS NO:372482-13-8
    4. Molecular Formula: C10H18N4O3
    5. Molecular Weight:
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 372482-13-8.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: 1-Pyrrolidinecarboxylic acid, 3-azido-4-methoxy-, 1,1-dimethylethyl ester, (3S,4S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Pyrrolidinecarboxylic acid, 3-azido-4-methoxy-, 1,1-dimethylethyl ester, (3S,4S)-(372482-13-8)
    11. EPA Substance Registry System: 1-Pyrrolidinecarboxylic acid, 3-azido-4-methoxy-, 1,1-dimethylethyl ester, (3S,4S)-(372482-13-8)
  • 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: 372482-13-8(Hazardous Substances Data)

372482-13-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 372482-13-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,2,4,8 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 372482-13:
(8*3)+(7*7)+(6*2)+(5*4)+(4*8)+(3*2)+(2*1)+(1*3)=148
148 % 10 = 8
So 372482-13-8 is a valid CAS Registry Number.

372482-13-8Relevant articles and documents

Highly active organocatalysts for asymmetric anti-mannich reactions

Martín-Rapún, Rafael,Fan, Xinyuan,Sayalero, Sonia,Bahramnejad, Mahboubeh,Cuevas, Félix,Pericàs, Miquel A.

supporting information; experimental part, p. 8780 - 8783 (2011/09/15)

Lighten the load! A family of enantiopure 4-oxy-substituted 3-aminopyrrolidines arising from the enantioselective ring-opening of meso-3-pyrroline oxide have been developed as catalysts for the asymmetric, anti-selective Mannich reaction (see scheme; PMP=

Design of novel aminopyrrolidine factor Xa inhibitors from a screening hit

Zbinden, Katrin Groebke,Anselm, Lilli,Banner, David W.,Benz, Joerg,Blasco, Francesca,Decoret, Guillaume,Himber, Jacques,Kuhn, Bernd,Panday, Narendra,Ricklin, Fabienne,Risch, Philippe,Schlatter, Daniel,Stahl, Martin,Thomi, Stefan,Unger, Robert,Haap, Wolfgang

body text, p. 2787 - 2795 (2009/10/17)

Starting from a hit identified by focused screening, 3-aminopyrrolidine factor Xa inhibitors were designed. The binding mode as determined by X-ray structural analysis as well as the pharmacokinetic behaviour of selected compounds is discussed.

Cyclic amines

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Page/Page column 37, (2010/11/24)

The invention is concerned with cyclic amines of formula (I) wherein X1 to X3, Y1 to Y3, R1′, R1″ and n are as defined in the description and in the claims, as well as physiologically acceptable salts thereof. These compounds inhibit coagulation factor Xa and can be used as medicaments and for treating diseases associated with coagulation factor Xa.

A short, simple and general approach for the synthesis of (3S,4S)-3-methoxy-4-methylamino pyrrolidine and (3S,4R)-3-methoxy-4-methylamino pyrrolidine

Kumar, A. Ravi,Reddy, J. Santhosh,Rao, B. Venkateswara

, p. 5687 - 5689 (2007/10/03)

A general and efficient stereoselective approach for the synthesis of (3S,4S) and (3S,4R)-3-methoxy-4-methylamino pyrrolidines, a part of the structure of AG-7352, a naphthyridine antitumor agent and quinoline antibacterial compounds has been described.

Efficient stereospecific synthesis of (S,S)-3-methoxy-4-methylaminopyrrolidine

Tsuzuki, Yasunori,Chiba, Katsumi,Hino, Katsuhiko

, p. 1793 - 1799 (2007/10/03)

Efficient stereospecific synthesis of (S,S)-3-methoxy-4-methylaminopyrrolidine, an important intermediate for a novel quinolone antitumor agent AG-7352 is presented. Starting from either D- or L-tartaric acid, a stereospecific synthesis of the chiral pyrrolidine was achieved via two SN2 displacement reactions. From the results of this synthetic study, the absolute structure of AG-7352 was chemically determined.

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