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N-benzyloxycarbonylalanylglycine ethyl ester, also known as Z-Ala-Gly-OEt, is a peptide derivative that consists of two amino acids, alanine and glycine, connected by a peptide bond. The N-benzyloxycarbonyl (Z) group is a protecting group attached to the amino group of alanine, which is commonly used in peptide synthesis to prevent unwanted side reactions. The ethyl ester group is attached to the carboxylic acid group of glycine, making it a water-soluble derivative. N-benzyloxycarbonylalanylglycine ethyl ester is often used as a building block in the synthesis of larger peptides and proteins, as well as in the study of peptide chemistry and drug development.

4905-31-1

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Basic information
1. Product Name: N-benzyloxycarbonylalanylglycine ethyl ester
2. Synonyms: N-benzyloxycarbonylalanylglycine ethyl ester
3. CAS NO:4905-31-1
4. Molecular Formula:
5. Molecular Weight: 308.334
6. EINECS: N/A
7. Product Categories: N/A
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: N-benzyloxycarbonylalanylglycine ethyl ester(CAS DataBase Reference)
10. NIST Chemistry Reference: N-benzyloxycarbonylalanylglycine ethyl ester(4905-31-1)
11. EPA Substance Registry System: N-benzyloxycarbonylalanylglycine ethyl ester(4905-31-1)
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: 4905-31-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 4905-31-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,0 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4905-31:
(6*4)+(5*9)+(4*0)+(3*5)+(2*3)+(1*1)=91
91 % 10 = 1
So 4905-31-1 is a valid CAS Registry Number.

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4905-31-1Relevant academic research and scientific papers

Design and Synthesis of Enkephalin Analogues: Part II - Synthesis of 2, Met5>-Enkephalin Alkylamides Having Morphinomimetic Activity

Dhotre, B. J.,Mathur, K. B.

, p. 1231 - 1236 (2007/10/02)

Alkylamides of 2, Met5>-enkephalin have been synthesized by two different routes.The first method consists of the sequential peptidation of Phe-Met-ONBzl by 2,4,5-trichlorophenyl esters of Boc-Gly, Boc-D-Ala and Boc-Tyr to get

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