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L-Proline, 1-[N-[(phenylmethoxy)carbonyl]glycyl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24277-16-5

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24277-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24277-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,7 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24277-16:
(7*2)+(6*4)+(5*2)+(4*7)+(3*7)+(2*1)+(1*6)=105
105 % 10 = 5
So 24277-16-5 is a valid CAS Registry Number.

24277-16-5Downstream Products

24277-16-5Relevant academic research and scientific papers

Dicarbonates: Convenient 4-dimethylaminopyridine catalyzed esterification reagents

Takeda,Akiyama,Nakamura,Takizawa,Mizuno,Takayanagi,Harigaya

, p. 1063 - 1066 (1994)

The DMAP (4-dimethylaminopyridine) catalyzed reaction of dialkyl dicarbonates la-e and carboxylic acids 2 afforded the corresponding esters 5 in good yield.

COMPOSITIONS AND METHODS FOR THE TREATMENT OF FUNGAL INFECTIONS

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Page/Page column 65, (2015/12/09)

Compositions and methods for the treatment of fungal infections including compounds containing a chemotaxis receptor ligand moiety and a polyene antifungal agent moiety are disclosed. In particular, compounds containing a polyene antifungal agent and a formyl peptide receptor ligand can be used in the treatment of fungal infections caused by a fungus of the genus Aspergillus or Candida.

Amides in one pot from Carboxylic Acids and Amines via Sulfinylamides

Bai, Jianfei,Zambron, Bartosz K.,Vogel, Pierre

supporting information, p. 604 - 607 (2014/04/03)

An efficient method has been developed for the direct amidification of carboxylic acids via sulfinylamides preformed in situ by the reaction of pure amines with prop-2- ene-1-sulfinyl chloride. The method can be applied to aliphatic acids, including pivalic acid, aromatic acids, and primary and secondary amines. It is compatible with acids bearing unprotected alcohol, phenol, and ketone moieties and applicable to the synthesis of peptides. It does not induce their a-epimerization.

BROAD SPECTRUM ANTIBIOTICS

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Page/Page column 165; 166, (2013/02/27)

Provided herein are antibacterial compounds, wherein the compounds in some embodiments have broad spectrum bioactivity. The compounds provided herein can in other embodiments overcome the resistance conferred by single amino acid mutations at defined posi

SYNTHESIS OF HBsAG SEGMENTS IN SOLUTION

Schoen, I.,Szirtes, T.,Rill, A.

, p. 751 - 773 (2007/10/02)

Immunization with segments (117-137 and 121-137) of the surface antigen of hepatitis B virus (HBsAg) had been reported to protect against HB infection.Therefore in addition to these peptides, HBsAg(124-137) and the three C-terminally amidated derivatives

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