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L-Val-L-Ile-L-Ala-OMe is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 37580-54-4 Structure
  • Basic information

    1. Product Name: L-Val-L-Ile-L-Ala-OMe
    2. Synonyms: L-Val-L-Ile-L-Ala-OMe
    3. CAS NO:37580-54-4
    4. Molecular Formula: C15H29N3O4
    5. Molecular Weight: 315.40846
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 37580-54-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: L-Val-L-Ile-L-Ala-OMe(CAS DataBase Reference)
    10. NIST Chemistry Reference: L-Val-L-Ile-L-Ala-OMe(37580-54-4)
    11. EPA Substance Registry System: L-Val-L-Ile-L-Ala-OMe(37580-54-4)
  • 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: 37580-54-4(Hazardous Substances Data)

37580-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37580-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,8 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 37580-54:
(7*3)+(6*7)+(5*5)+(4*8)+(3*0)+(2*5)+(1*4)=134
134 % 10 = 4
So 37580-54-4 is a valid CAS Registry Number.

37580-54-4Downstream Products

37580-54-4Relevant articles and documents

Ethyl 2-cyano-2-(2-nitrobenzenesulfonyloxyimino)acetate (o -NosylOXY): A recyclable coupling reagent for racemization-free synthesis of peptide, amide, hydroxamate, and ester

Dev, Dharm,Palakurthy, Nani Babu,Thalluri, Kishore,Chandra, Jyoti,Mandal, Bhubaneswar

, p. 5420 - 5431 (2014/07/08)

Ubiquitousness of amide and ester functionality makes coupling reactions extremely important. Although numerous coupling reagents are available, methods of preparation of the common and efficient reagents are cumbersome. Those reagents generate a substantial amount of chemical waste and lack recyclability. Ethyl 2-cyano-2-(2-nitrobenzenesulfonyloxyimino)acetate (o-NosylOXY), the first member of a new generation of coupling reagents, produces byproducts that can be easily recovered and reused for the synthesis of the same reagent, making the method more environmentally friendly and cost-effective. The synthesis of amides, hydroxamates, peptides, and esters using this reagent is described. The synthesis of the difficult sequences, for example, the islet amyloid polypeptide (22-27) fragment (with a C-terminal Gly, H-Asn-Phe-Gly-Ala-Ile-Leu-Gly-NH 2) and acyl carrier protein (65-74) fragment (H-Val-Gln-Ala-Ala-Ile- Asp-Tyr-Ile-Asn-Gly-OH), following the solid-phase peptide synthesis (SPPS) protocol and Amyloid β (39-42) peptide (Boc-Val-Val-IIe-Ala-OMe), following solution-phase strategy is demonstrated. Remarkable improvement is noticed with respect to reaction time, yield, and retention of stereochemistry. A mechanistic investigation and recyclability are also described.

Synthesis and biological evaluation of potential bisubstrate inhibitors of protein farnesyltransferase. Design and synthesis of functionalized imidazoles

De Figueiredo, Renata Marcia,Coudray, Laetitia,Dubois, Joelle

, p. 3299 - 3309 (2008/09/20)

A novel series of compounds, derived from 2,5-functionalized imidazoles, have been synthesized as potential bisubstrate inhibitors of protein farnesyltransferase (FTase) using structure-based design. These compounds have a 1,4-diacid chain and a tripeptid

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