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Carbamic acid, (2-oxo-3-phenylpropyl)-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 162536-89-2 Structure
  • Basic information

    1. Product Name: Carbamic acid, (2-oxo-3-phenylpropyl)-, 1,1-dimethylethyl ester
    2. Synonyms:
    3. CAS NO:162536-89-2
    4. Molecular Formula: C14H19NO3
    5. Molecular Weight: 249.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 162536-89-2.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: Carbamic acid, (2-oxo-3-phenylpropyl)-, 1,1-dimethylethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, (2-oxo-3-phenylpropyl)-, 1,1-dimethylethyl ester(162536-89-2)
    11. EPA Substance Registry System: Carbamic acid, (2-oxo-3-phenylpropyl)-, 1,1-dimethylethyl ester(162536-89-2)
  • 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: 162536-89-2(Hazardous Substances Data)

162536-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162536-89-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,5,3 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 162536-89:
(8*1)+(7*6)+(6*2)+(5*5)+(4*3)+(3*6)+(2*8)+(1*9)=142
142 % 10 = 2
So 162536-89-2 is a valid CAS Registry Number.

162536-89-2Downstream Products

162536-89-2Relevant articles and documents

A Novel Entry to 3,4,5-Trisubstituted 2-Pyrrolidones from Isoxazoline-N-oxides

Zhmurov, Petr A.,Ushakov, Pavel Yu.,Novikov, Roman A.,Sukhorukov, Alexey Yu.,Ioffe, Sema L.

, p. 1871 - 1874 (2018)

A novel strategy for the synthesis of stereochemically defined 3,4,5-trisubstituted 2-pyrrolidones was developed. The suggested approach involves reductive domino-type recyclization of 3-aminomethyl-substituted isoxazolines as a key stage. The latter are prepared via α-C-H functionalization of readily available isoxazoline-N-oxides.

Nickel-Catalyzed Cross-Coupling of Alkyl Carboxylic Acid Derivatives with Pyridinium Salts via C-N Bond Cleavage

Pulikottil, Feba Thomas,Pilli, Ramadevi,Suku, Rohith Valavil,Rasappan, Ramesh

, p. 2902 - 2907 (2020/04/09)

The electrophile-electrophile cross-coupling of carboxylic acid derivatives and alkylpyridinium salts via C-N bond cleavage is developed. The method is distinguished by its simplicity and steers us through a variety of functionalized ketones in good to excellent yields. Besides acid chlorides, carboxylic acids were also employed as acylating agents, which enabled us to incorporate acid-sensitive functional groups such as MOM, BOC, and acetal. Control experiments with TEMPO revealed a radical pathway.

Asymmetric hydrogenation of protected allylic amines

Steinhuebel, Dietrich P.,Krska, Shane W.,Alorati, Anthony,Baxter, Jenny M.,Belyk, Kevin,Bishop, Brian,Palucki, Michael,Sun, Yongkui,Davies, Ian W.

supporting information; experimental part, p. 4201 - 4203 (2010/11/19)

A general method for the enantioselective hydrogenation of protected allylic amine derivatives is described. This procedure relies on the generation of a cationic ruthenium complex with the axially chiral ligand (-)-TMBTP. The utility is highlighted by th

INHIBITORS OF Akt ACTIVITY

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Page/Page column 191, (2010/11/27)

Invented are novel thiophene compounds, the use of such compounds as inhibitors of protein kinase B activity and in the treatment of cancer and arthritis.

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