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63276-44-8

TFA*H-Lys(Z)-Gly-OMe is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 63276-44-8 Structure

  • Basic information

    1. Product Name: TFA*H-Lys(Z)-Gly-OMe
    2. Synonyms: TFA*H-Lys(Z)-Gly-OMe
    3. CAS NO:63276-44-8
    4. Molecular Formula:
    5. Molecular Weight: 465.427
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 63276-44-8.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: TFA*H-Lys(Z)-Gly-OMe(CAS DataBase Reference)
    10. NIST Chemistry Reference: TFA*H-Lys(Z)-Gly-OMe(63276-44-8)
    11. EPA Substance Registry System: TFA*H-Lys(Z)-Gly-OMe(63276-44-8)

  • 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: 63276-44-8(Hazardous Substances Data)

63276-44-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63276-44-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,7 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63276-44:
(7*6)+(6*3)+(5*2)+(4*7)+(3*6)+(2*4)+(1*4)=128
128 % 10 = 8
So 63276-44-8 is a valid CAS Registry Number.

63276-44-8Relevant articles and documents

MODIFIED MACROMOLECULE

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Page/Page column 110-111; 22/28, (2008/06/13)

The present invention relates to a macromolecule having a controlled terminal group stoichiometry, the macromolecule including a surface layer, at least one subsurface layer and at least two terminal groups including: a first terminal group which is a res

Solution-phase synthesis of an anti-human immunodeficiency virus peptide, T22 ([Tyr5,12, Lys7]-polyphemusin II), and the modification of Trp by the p-methoxybenzyl group of cys during trimethylsilyl trifluoromethanesulfonate deprotec

Tamamura,Otaka,Takada,Terakawa,Yoshizawa,Masuda,Ibuka,Murakami,Nakashima,Waki,Matsumoto,Yamamoto,Fujii

, p. 12 - 18 (2007/10/02)

T22 ([Tyr5,12, Lys7]-polyphemusin II) was previously synthesized by a solid-phase method and was found to have a strong anti-human immunodeficiency virus (HIV) activity, comparable to that of 3'-azido-2',3'-dideoxy- thymidine (AZT).

Synthesis of a Cyclic Peptide Polyamine: A Comparative Study of Routes to Cyclo-(Lys-Lys-Gly)2

Bailey, Patrick D.,Crofts, Gavin A.

, p. 3207 - 3210 (2007/10/02)

Several methods for the preparation of cyclo-(Lys-Lys-Gly)2 were compared.Cyclisation of linear hexapeptides of the type H-2-X was most efficient using excess DPPA with the free amino acid (i.e.X = OH), but purification and scale-up wer

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