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acetyl leucine enkephalin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78922-82-4

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78922-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78922-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,2 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78922-82:
(7*7)+(6*8)+(5*9)+(4*2)+(3*2)+(2*8)+(1*2)=174
174 % 10 = 4
So 78922-82-4 is a valid CAS Registry Number.

78922-82-4Downstream Products

78922-82-4Relevant academic research and scientific papers

A rapid reaction releasing the carboxyl terminal residues of peptides

Yagisawa, Shiroki,Urakami, Masako

, p. 7557 - 7560 (1996)

Alcoholysis of peptide oxazolones in alcohols containing dilute acid, such as 0.02M HCl, gives the C-terminal amino acid and the ester of the shortened peptide within 10 minutes at room temperature in 30-70% yields. This together with the finding that the peptide oxazolones can be formed within 3 minutes with alkylchloroformates enables the rapid removal of peptide C-terminal residues.

Structural Studies of Polyhydroxybis(tetrahydrofuran)acetogenins from Annona squamosa Using the Combination of Chemical Derivatization and Precursor-ion Scanning Mass Spectrometry

Hirayama, Kazuo,Akashi, Satoko,Yuji, Reiko,Niitsu, Uno,Fujimoto, Yoshinori

, p. 1516 - 1524 (1993)

The structure of squamocin polyhydroxybis(tetrahydrofuran)acetogenin from Annona squamosa L., was characterized by a combination of the chemical derivatization and precursor-ion scanning mass spectrometry.The lactone part of squamocin was modified with N,N-dimethylethylenediamine in the vapour phase to afford a strong positive charge at one end of the skeleton.The derivative was ionized by fast atom bombardment (FAB), and the product-ion spectrum from (+) and the precursor ion spectrum from the m/z 72 ion generated by low-energy collision were acquired.The structure of the derivative could be characterized by the precursor-ion spectrum from the m/z 72 ion, but little structural information could be obtained from the product-ion spectrum from (+) of the derivative.By the attachment of a tertiary amino group to one end of the skeleton, charge-remote fragmentation was facilitated and abundant and unique fragment ions were observed in the precursor-ion spectrum.Structural characterization of six other isolated compounds was also carried out, and two novel compounds were found by this technique.A similar derivatization was applied in the peptide leu-enkephalin, and full sequencing from the C-terminus using precursor-ion scanning from m/z 72 could be achieved.

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