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methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate

    Cas No: 96363-21-2

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  • 96363-21-2 Structure
  • Basic information

    1. Product Name: methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate
    2. Synonyms: methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate
    3. CAS NO:96363-21-2
    4. Molecular Formula:
    5. Molecular Weight: 309.362
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 96363-21-2.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: methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate(96363-21-2)
    11. EPA Substance Registry System: methyl D,L-3-<<(1,1-dimethylethoxy)carbonyl>amino>-3-(4-methoxyphenyl)propanoate(96363-21-2)
  • 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: 96363-21-2(Hazardous Substances Data)

96363-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96363-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,3,6 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 96363-21:
(7*9)+(6*6)+(5*3)+(4*6)+(3*3)+(2*2)+(1*1)=152
152 % 10 = 2
So 96363-21-2 is a valid CAS Registry Number.

96363-21-2Relevant articles and documents

Synthesis of macrocycles containing 1,3,4-oxadiazole and pyridine moieties

Poojari, Subba,Naik, Parameshwar,Krishnamurthy

, p. 305 - 309 (2014/01/06)

A series of peptide-like 25-28 membered macrocycles containing 1,3,4-oxadiazoles and pyridines bearing a chiral center scaffold have been synthesized by using known coupling reagents and common protecting groups. The yield of the purified macrocycles was poor on an average, yet it seems to be independent of amino acid substitution or stereochemistry. These macrocycles represent a new class of structures for further development and for future application in high-throughput screening against a variety of biological targets.

Total Synthesis of 2'-Deoxymugineic Acid and Nicotianamine

Matsuura, Fumiyoshi,Hamada, Yasumasa,Shioiri, Takayuki

, p. 9457 - 9470 (2007/10/02)

Steroselective total synthesis of the unique phytosiderophores, 2'-deoxymugineic acid (4) and nicotianamine (5), has been achieved from the β-tyrosine derivative 21 using its aryl groups as the carboxyl synthon.

Synthesis of (4R)-D,L-- and (4S)-D,L-Homoserine Lactones

Kalvin, Douglas M.,Woodard, Ronald W.

, p. 2259 - 2263 (2007/10/02)

The (4R)-D,L-- and (4S)-D,L-homoserine lactone hydrochloride salts were prepared from D,L-3-amino-3-(4-methoxyphenyl)propanoic acid (1) in eight steps in an overall yields of 5.0percent.Amino acid 1 was converted into D,L-3-(1,1-dimethyletho

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