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cyclo-D-tyrosyl-L-tyrosine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10125-12-9 Structure
  • Basic information

    1. Product Name: cyclo-D-tyrosyl-L-tyrosine
    2. Synonyms: cyclo-D-tyrosyl-L-tyrosine
    3. CAS NO:10125-12-9
    4. Molecular Formula:
    5. Molecular Weight: 326.352
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10125-12-9.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: cyclo-D-tyrosyl-L-tyrosine(CAS DataBase Reference)
    10. NIST Chemistry Reference: cyclo-D-tyrosyl-L-tyrosine(10125-12-9)
    11. EPA Substance Registry System: cyclo-D-tyrosyl-L-tyrosine(10125-12-9)
  • 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: 10125-12-9(Hazardous Substances Data)

10125-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10125-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,2 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10125-12:
(7*1)+(6*0)+(5*1)+(4*2)+(3*5)+(2*1)+(1*2)=39
39 % 10 = 9
So 10125-12-9 is a valid CAS Registry Number.

10125-12-9Downstream Products

10125-12-9Relevant articles and documents

MODULUS MODIFIERS AND FILMS THEREOF

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Paragraph 0206-0207, (2022/01/12)

The present disclosure relates to compositions derived from bioreachable molecules, such as amino acids and/or steroids. In particular, the composition can be a monomer, a polymer, or a copolymer derived from an amino acid dimer. Such compositions can optionally include a functionalized steroid.

Heterogeneous Catalytic Hydrogenation of Chiral Amino Acid Methyl Esters to Amino Alcohols with Retention of Configuration Over Mg-Modified Cu/ZnO/Al2O3 Catalyst

Zhan, Bing,Zhang, Shuangshuang,Yu, Jun,Xiao, Xiuzheng,Guo, Xiaoming,Mao, Dongsen,Lu, Guanzhong

, p. 2160 - 2166 (2017/07/25)

Selective hydrogenation of amino acid methyl esters to chiral amino alcohols is an important and fascinating process. The CuZn0.3Mg0.1AlOx catalyst for the synthesis of chiral amino alcohols was prepared by the fractional

Intramolecular Interaction of Porphyrin Moieties in 2,5-Piperazinedione-Bridged Porphyrin Dimers

Tamiaki, Hitoshi,Suzuki, Shinji,Maruyama, Kazuhiro

, p. 2633 - 2637 (2007/10/02)

Diastereomerically pure 2,5-piperazinedione-bridged meso-tetraarylporphyrin dimers were synthesized with easy procedures. 1H NMR, UV-vis, and CD spectra showed that porphyrin moieties in the L,L-molecule interacted more strongly than those in the D,L-isom

Pyrazine Chemistry. II. Reduction of 3,6-Dibenzylidenepiperazine-2,5-diones

Marcuccio, Sebastian M.,Elix, John A.

, p. 1791 - 1794 (2007/10/02)

A reinvestigation of the reduction of 3,6-dibenzylidenepiperazine-2,5-dione (1) with zinc and acetic acid established that this reaction gave (Z)-6-benzyl-3-benzylidenepiperazine-2,5-dione (10).When a mixture of acetic acid and hydrochloric acid was used

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