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183119-28-0

tert-butyl (R)-4-((R)-2-(methoxycarbonyl)-1-phenylethyl)-2,2-dimethyloxazolidine-3-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 183119-28-0 Structure

  • Basic information

    1. Product Name: tert-butyl (R)-4-((R)-2-(methoxycarbonyl)-1-phenylethyl)-2,2-dimethyloxazolidine-3-carboxylate
    2. Synonyms: tert-butyl (R)-4-((R)-2-(methoxycarbonyl)-1-phenylethyl)-2,2-dimethyloxazolidine-3-carboxylate
    3. CAS NO:183119-28-0
    4. Molecular Formula:
    5. Molecular Weight: 363.454
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 183119-28-0.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: tert-butyl (R)-4-((R)-2-(methoxycarbonyl)-1-phenylethyl)-2,2-dimethyloxazolidine-3-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl (R)-4-((R)-2-(methoxycarbonyl)-1-phenylethyl)-2,2-dimethyloxazolidine-3-carboxylate(183119-28-0)
    11. EPA Substance Registry System: tert-butyl (R)-4-((R)-2-(methoxycarbonyl)-1-phenylethyl)-2,2-dimethyloxazolidine-3-carboxylate(183119-28-0)

  • 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: 183119-28-0(Hazardous Substances Data)

183119-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183119-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,1,1 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 183119-28:
(8*1)+(7*8)+(6*3)+(5*1)+(4*1)+(3*9)+(2*2)+(1*8)=130
130 % 10 = 0
So 183119-28-0 is a valid CAS Registry Number.

183119-28-0Relevant articles and documents

Stereocontrolled sequential functionalization in acyclic systems by exploiting internal 1,2-asymmetric induction - Generation of symmetry-related polyamino alcohol motifs

Hanessian, Stephen,Wang, Wengui,Gai, Yonghua

, p. 7477 - 7480 (1996)

Treatment of acyclic γ-ureido α,β-unsaturated esters with lithium dialkyl or diaryl cuprates leads to the corresponding β,γ-substituted esters with high syn-stereoselectivity. The potassium enolates of these compounds react with trisyl azide or the Davis

A solution to the stereochemical problems posed by amaryllidaceae constituents using a highly syn-selective arylcuprate conjugate addition to γ-amino and γ-carbamato-α,β-enoates

Rastogi, Shiva K.,Kornienko, Alexander

, p. 3170 - 3178 (2007/10/03)

Various substituted arylcuprates undergo stereocontrolled additions to l-serine-derived γ-amino- and γ-carbamato-α,β-enoates with high syn-selectivities. The stereochemical outcome of these reactions is fully consistent with the reductive elimination-base

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