111491-74-8

Basic information

• Product Name: C₅₀H₇₅N₉O₁₂S
• Synonyms: C₅₀H₇₅N₉O₁₂S
• CAS NO: 111491-74-8
• Molecular Weight: 1026.26
• Mol File: 111491-74-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₅₀H₇₅N₉O₁₂S(CAS DataBase Reference)
• NIST Chemistry Reference: C₅₀H₇₅N₉O₁₂S(111491-74-8)
• EPA Substance Registry System: C₅₀H₇₅N₉O₁₂S(111491-74-8)

Safety Data

• Hazardous Substances Data: 111491-74-8(Hazardous Substances Data)

Upstream product

• 111491-72-6 (S)-1-(2-{[(S)-1-((S)-2-Benzyloxycarbonylamino-3-phenyl-propionyl)-pyrrolidine-2-carbonyl]-amino}-acetyl)-pyrrolidine-2-carboxylic acid tert-butyl ester 
• 147-85-3 L-proline 
• 24692-53-3 N^α-benzoyloxycarbonyl(γ-O-tert-butyl)glutamylhistidine methyl ester 
• 3967-22-4 N^α-benzyloxycarbonyl(γ-tert-butyl)glutamylhistidine methyl ester 
• 4467-54-3 l-histidine methyl ester dihydrochloride 
• 7669-64-9 (2S)-1-((2S)-2-[[(benzyloxy)carbonyl]amino]-3-phenylpropanoyl)tetrahydro-1H-pyrrole-2-carboxylic acid 
• 111491-71-5 (S)-1-[2-(Trityl-amino)-acetyl]-pyrrolidine-2-carboxylic acid tert-butyl ester 
• 60166-68-9 glycylproline tert-butyl ester 
• 5497-76-7 L-proline tert-butyl ester hydrochloride 
• 3886-08-6 5-tert-butyl N-benzyloxycarbonyl-L-glutamate 
• 1161-13-3 N-Cbz-L-Phe 
• 111491-73-7 phenylalanylprolylglycylproline tert-butyl ester 
• 24734-96-1 (S)-4-((S)-2-tert-Butoxycarbonylamino-4-methylsulfanyl-butyrylamino)-4-[(S)-1-hydrazinocarbonyl-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-butyric acid tert-butyl ester 

Downstream Products

• 80714-61-0 H-Met-Glu-His-Phe-Pro-Gly-Pro 

Relevant articles and documents

SYNTHESIS OF A HEPTAPEPTIDE FORMING A MODIFIED ACTH 4-10 FRAGMENT

A scheme is given for the synthesis of a heptapeptide representing a modified ACTH 4-10 fragment on the basis of which it is possible to create a preparation that is an effective adaptogen of peptide nature.A proposed variant of the synthesis permits a peptide with an adequate degree of purity to be obtained comparatively simply on a large scale.The intermediate compunds and the final products were obtained with good yields and were distinguished by chromatographic homogeneity.The heptapeptide synthesized did not differ with respect to its physicochemical characteristics and biological action from the analogous compound obtained previously.Some physicochemical characteristics of the compound obtained (angles of optical rotation, chromatographic mobilities) are given.