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5-BENZYLOXYMETHYL-OXAZOLIDIN-2-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 134580-97-5 Structure
  • Basic information

    1. Product Name: 5-BENZYLOXYMETHYL-OXAZOLIDIN-2-ONE
    2. Synonyms: 5-BENZYLOXYMETHYL-OXAZOLIDIN-2-ONE
    3. CAS NO:134580-97-5
    4. Molecular Formula: C11H13NO3
    5. Molecular Weight: 207.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 134580-97-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 5-BENZYLOXYMETHYL-OXAZOLIDIN-2-ONE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-BENZYLOXYMETHYL-OXAZOLIDIN-2-ONE(134580-97-5)
    11. EPA Substance Registry System: 5-BENZYLOXYMETHYL-OXAZOLIDIN-2-ONE(134580-97-5)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 134580-97-5(Hazardous Substances Data)

134580-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134580-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,5,8 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134580-97:
(8*1)+(7*3)+(6*4)+(5*5)+(4*8)+(3*0)+(2*9)+(1*7)=135
135 % 10 = 5
So 134580-97-5 is a valid CAS Registry Number.

134580-97-5Relevant articles and documents

Aluminium-Catalysed Oxazolidinone Synthesis and their Conversion into Functional Non-Symmetrical Ureas

Laserna, Victor,Guo, Wusheng,Kleij, Arjan W.

, p. 2849 - 2854 (2015/09/28)

An efficient and practical aluminium-catalysed approach towards a range of functional oxazolidinones is reported. The method is based on cheap and readily available starting materials including terminal and internal (bicyclic) epoxides and phenyl carbamate. The oxazolidinones serve as highly useful synthons for the high yield preparation of non-symmetrical ureas by nucleophilic ring-opening affording the targeted urea compounds with excellent functional group diversity, high regioselectivity and isolated yields up to >99%.

GSK-3BETA INHIBITOR

-

Page/Page column 30-31, (2011/04/13)

For the purpose of providing a GSK-3β inhibitor containing a 2-aminopyridine compound or a salt thereof or a prodrug thereof useful as an agent for the prophylaxis or treatment of a GSK-3β-related pathology or disease, the present invention provides a GSK-3β inhibitor containing a compound represented by the formula (IA): wherein each symbol is as defined in the specification. or a salt thereof or a prodrug thereof.

A facile one-pot solid-phase synthesis of oxazolidin-2-ones using polymer-supported 2-hydroxyalkyl selenide reagent

Hu, Qiao-Sheng,Sheng, Shou-Ri,Lin, Shu-Ying,Wei, Mei-Hong,Xin, Qin,Liu, Xiao-Ling

, p. 74 - 75 (2008/02/04)

A simple, efficient and environmentally friendly procedure for one-pot solid-phase synthesis of 2-oxazolidinones in moderate to good yields by reaction of polystyrene-supported 2-hydroxyalkyl selenide with benzoyl isocyanate and subsequent oxidation/cycli

Facile one-pot synthesis of oxazolidin-2-ones from phenyl 2-hydroxyalkyl selenides

Sheng, Shou-Ri,Luo, Hai-Rong,Huang, Zhen-Zhong,Sun, Wu-Kang,Liu, Xiao-Ling

, p. 2693 - 2699 (2008/02/12)

A novel, convenient, efficient, three-step, one-pot synthesis of 2-oxazolidinones from phenyl 2-hydroxyalkyl selenides was developed. Using this methodology, 2-oxazolidinones are obtained in good yields (76-85%) by reaction of phenyl 2-hydroxyalkyl seleni

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