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CAS

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259822-63-4

methyl (2S)-2-amino-4-(tritylsulfanyl)butanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 259822-63-4 Structure

  • Basic information

    1. Product Name: methyl (2S)-2-amino-4-(tritylsulfanyl)butanoate
    2. Synonyms: methyl (2S)-2-amino-4-(tritylsulfanyl)butanoate
    3. CAS NO:259822-63-4
    4. Molecular Formula:
    5. Molecular Weight: 391.534
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 259822-63-4.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: methyl (2S)-2-amino-4-(tritylsulfanyl)butanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl (2S)-2-amino-4-(tritylsulfanyl)butanoate(259822-63-4)
    11. EPA Substance Registry System: methyl (2S)-2-amino-4-(tritylsulfanyl)butanoate(259822-63-4)

  • 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: 259822-63-4(Hazardous Substances Data)

259822-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 259822-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,8,2 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 259822-63:
(8*2)+(7*5)+(6*9)+(5*8)+(4*2)+(3*2)+(2*6)+(1*3)=174
174 % 10 = 4
So 259822-63-4 is a valid CAS Registry Number.

259822-63-4Relevant articles and documents

Cyclic thioether peptide mimetics as VCAM-VLA-4 antagonists

Fotouhi, Nader,Joshi, Pramod,Tilley, Jefferson W.,Rowan, Karen,Schwinge, Virginia,Wolitzky, Barry

, p. 1167 - 1169 (2007/10/03)

Selective substitution of a sulfur atom by carbon in a highly potent 13-membered cyclic disulfide was accomplished by intramolecular displacement of a bromide. The potency of the resulting thioethers in the VCAM/VLA-4 assay was dependant on ring size and the position of the sulfur atom. (C) 2000 Elsevier Science Ltd. All rights reserved.

The first asymmetric syntheses of L-homocysteine and L-homocystine

Adamczyk, Maciej,Fishpaugh, Jeffrey R.,Thiruvazhi, Mohan

, p. 4151 - 4156 (2007/10/03)

Asymmetric syntheses of L-homocysteine 1 and L-homocystine 2 are described. Alkylation of the carbanion derived from Schollkopf reagent 3 and ensuing hydrolyses gave S-triphenylmethyl-L-homocysteine 6. Removal of the triphenylmethyl group gave L-homocysteine 1 and subsequent oxidation provided L-homocystine 2.

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