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Pentanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-5-[[(4-methylphenyl)sulfonyl]oxy] -, methyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 130223-39-1 Structure
  • Basic information

    1. Product Name: Pentanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-5-[[(4-methylphenyl)sulfonyl]oxy] -, methyl ester, (S)-
    2. Synonyms:
    3. CAS NO:130223-39-1
    4. Molecular Formula: C18H27NO7S
    5. Molecular Weight: 401.481
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 130223-39-1.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: Pentanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-5-[[(4-methylphenyl)sulfonyl]oxy] -, methyl ester, (S)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Pentanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-5-[[(4-methylphenyl)sulfonyl]oxy] -, methyl ester, (S)-(130223-39-1)
    11. EPA Substance Registry System: Pentanoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-5-[[(4-methylphenyl)sulfonyl]oxy] -, methyl ester, (S)-(130223-39-1)
  • 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: 130223-39-1(Hazardous Substances Data)

130223-39-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130223-39-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,2,2 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 130223-39:
(8*1)+(7*3)+(6*0)+(5*2)+(4*2)+(3*3)+(2*3)+(1*9)=71
71 % 10 = 1
So 130223-39-1 is a valid CAS Registry Number.

130223-39-1Relevant articles and documents

TLR2 MODULATOR COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF

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, (2021/12/08)

The present disclosure relates to compounds which modulate the activity of Toll-like receptor (TLR) proteins, including agonists or activators, partial agonists, and antagonists. Of particular interest of compounds that modulate the activity of TLR2, as well as methods of using such compounds to treat cancer and other disorders associated with a TLR2 pathway.

HALOARYL SUBSTITUTED AMINOPURINES, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH

-

Page/Page column 151, (2008/06/13)

Provided herein are Aminopurine Compounds having the following structure: (I) wherein R1 , R2 and and R3 are as defined herein, compositions comprising an effective amount of an Aminopurine Compound and methods for treating or preventing cancer, a cardiovascular disease, a renal disease, an autoimmune condition, an inflammatory condition, macular degeneration, ischemia-reperfusion injury, pain and related syndromes, disease-related wasting, an asbestos-related condition, pulmonary hypertension or a condition treatable or preventable by inhibition of the JNK pathway comprising administering an effective amount of an Aminopurine Compound to a patient in need thereof.

Synthesis of enantiomerically pure β- and γ-amino acids from aspartic and glutamic acid derivatives

El Marini,Roumestant,Viallefont,Razafindramboa,Bonato,Follet

, p. 1104 - 1108 (2007/10/02)

An efficient synthesis of enantiomerically pure β- and γ-amino acids starting from commercially available aspartic and glutamic acid derivatives is described. The acid function, α to the amino group, is first transformed to a good leaving group and the pr

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