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benzyl 3-oxocyclopentylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 635311-42-1 Structure
  • Basic information

    1. Product Name: benzyl 3-oxocyclopentylcarbamate
    2. Synonyms: benzyl 3-oxocyclopentylcarbamate;benzyl N-(3-oxocyclopentyl)carbamate;β-benzyloxycarbonylamino-cyclopentanone
    3. CAS NO:635311-42-1
    4. Molecular Formula: C13H15NO3
    5. Molecular Weight: 233.2631
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 635311-42-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 415.0±44.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.19±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 11.69±0.20(Predicted)
    10. CAS DataBase Reference: benzyl 3-oxocyclopentylcarbamate(CAS DataBase Reference)
    11. NIST Chemistry Reference: benzyl 3-oxocyclopentylcarbamate(635311-42-1)
    12. EPA Substance Registry System: benzyl 3-oxocyclopentylcarbamate(635311-42-1)
  • 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: 635311-42-1(Hazardous Substances Data)

635311-42-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 635311-42-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,5,3,1 and 1 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 635311-42:
(8*6)+(7*3)+(6*5)+(5*3)+(4*1)+(3*1)+(2*4)+(1*2)=131
131 % 10 = 1
So 635311-42-1 is a valid CAS Registry Number.

635311-42-1Relevant articles and documents

HETEROCYCLIC COMPOUNDS AS KINASE INHIBITORS

-

, (2021/01/23)

Heterocyclic compounds as CDK4 or CDK6 or other CDK inhibitors are provided. The compounds may find use as therapeutic agents for the treatment of diseases and may find particular use in oncology.

Oxyfunctionalization of the Remote C?H Bonds of Aliphatic Amines by Decatungstate Photocatalysis

Schultz, Danielle M.,Lévesque, Fran?ois,DiRocco, Daniel A.,Reibarkh, Mikhail,Ji, Yining,Joyce, Leo A.,Dropinski, James F.,Sheng, Huaming,Sherry, Benjamin D.,Davies, Ian W.

, p. 15274 - 15278 (2017/11/01)

Aliphatic amines, oxygenated at remote positions within the molecule, represent an important class of synthetic building blocks to which there are currently no direct means of access. Reported herein is an efficient and scalable solution that relies upon decatungstate photocatalysis under acidic conditions using either H2O2 or O2 as the terminal oxidant. By using these reaction conditions a series of simple and unbiased aliphatic amine starting materials can be oxidized to value-added ketone products. Lastly, NMR spectroscopy using in situ LED-irradiated samples was utilized to monitor the kinetics of the reaction, thus enabling direct translation of the reaction into flow.

THERAPEUTICALLY ACTIVE COMPOUNDS AND THEIR METHODS OF USE

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Page/Page column, (2015/03/31)

Provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH1/2 comprising administering to a subject in need thereof a compound described here.

POTENT SMALL MOLECULE INHIBITORS OF AUTOPHAGY, AND METHODS OF USE THEREOF

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Page/Page column 138, (2014/09/29)

Certain aspects of the invention relate to small molecule autophagy inhibitors, and their use for treatment and prevention of cancers and acute pancreatitis. Medicinal chemistry studies led to small molecular autophagy inhibitors with improved potency and selectivity.

THERAPEUTICALLY ACTIVE COMPOUNDS AND THEIR METHODS OF USE

-

Page/Page column 44, (2013/07/31)

Provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH1/2 comprising administering to a subject in need thereof a compound described here.

Microwave-assisted synthesis of novel (5-nitropyridin-2-yl)alkyl and (5-nitropyridin-3-yl)alkyl carbamates

Henry, Christophe,Haupt, Andreas,Turner, Sean C.

supporting information; experimental part, p. 1932 - 1938 (2009/08/07)

A straightforward approach to novel (5-nitropyridin-2-yl)alkyl and (5-nitropyridin-3-yl)alkyl carbamate building blocks is presented in this study. Their construction is achieved by condensation of N-carbamate a- and β-amino carbonyl derivatives with l-methyl-3,5-dinitro-2-pyridone 1 under microwave irradiation. Judiciously chosen modifications in the nature of the parent carbonyl starting material has influenced the regiochemical outcome of the reaction and allowed an efficient access to novel nitrogen-containing scaffolds. Compounds sharing morphological similarities have been gathered in three libraries differing from each other in a single structural parameter.

HETEROCYCLIC CETP INHIBITORS

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Page/Page column 118, (2010/11/27)

Compounds of formula Ia and Ib wherein A, B, C and R1 are described herein.

Highly efficient phosphine-catalyzed aza-Michael reactions of α,β-unsaturated compounds with carbamates in the presence of TMSCl

Xu, Li-Wen,Xia, Chun-Gu

, p. 4507 - 4510 (2007/10/03)

Aza-Michael reactions of enones with carbamates took place efficiently in the presence of a catalytic amount of phosphine and TMSCl to afford the total products in high yields. The new catalytic system was also efficient in the aza-Michael reaction of chalcone, which was difficult to react with carbamates by transition metal salts catalysts.

Highly Efficient Aza-Michael Reactions of Enones with Carbamates Using a Combination of Quaternary Ammonium Salts and BF3·OEt 2 as a Catalyst

Xu, Li-Wen,Li, Lyi,Xia, Chun-Gu,Zhou, Shao-Lin,Li, Jing-Wei,Hu, Xiao-Xue

, p. 2337 - 2340 (2007/10/03)

Aza-Michael reactions of enones with carbamates took efficiently in the presence of a catalytic amount of quaternary ammonium salts and BF 3·OEt2 to afford the total products in high yields. The new catalytic system was also efficient in the aza-Michael reaction of chalcone, which was difficult to react with carbamates by transition metal salts catalysts.

An efficient and inexpensive catalyst system for the aza-Michael reactions of enones with carbamates

Xu, Li-Wen,Xia, Chun-Gu,Hu, Xiao-Xue

, p. 2570 - 2571 (2007/10/03)

A new strategy which uses very cheap FeCl3 as an effective catalyst in the presence of Me3SiCl has been developed for the conjugate addition of enones and chalcone with unactivated weakly nucleophilic carbamates.

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