Cas 292141-31-2,AC-D-2-NAL-4-CHLORO-D-PHE-BETA-(3-PYRIDYL)-D-ALA-GLY-ARG-PRO-D-ALA-NH2

292141-31-2

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Basic information

Product Name: AC-D-2-NAL-4-CHLORO-D-PHE-BETA-(3-PYRIDYL)-D-ALA-GLY-ARG-PRO-D-ALA-NH2
Synonyms: AC-D-2-NAL-4-CHLORO-D-PHE-BETA-(3-PYRIDYL)-D-ALA-GLY-ARG-PRO-D-ALA-NH2;AC-D-ALA(2-NAPHTHYL)-D-PHE(4-CL)-D-ALA(3'-PYRIDYL)-GLY-ARG-PRO-D-ALA-NH2;LUTEINIZING HORMONE-RELEASING HORMONE ANTAGONIST;Ac-D-2-Nal-p-chloro-D-Phe-b-(3-pyridyl)-D-Ala-Gly-Arg-Pro-D-Ala-NH2
CAS NO:292141-31-2
Molecular Formula: C48H59ClN12O8
Molecular Weight: 967.51
EINECS: N/A
Product Categories: N/A
Mol File: 292141-31-2.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: -15°C
Solubility: N/A
CAS DataBase Reference: AC-D-2-NAL-4-CHLORO-D-PHE-BETA-(3-PYRIDYL)-D-ALA-GLY-ARG-PRO-D-ALA-NH2(CAS DataBase Reference)
NIST Chemistry Reference: AC-D-2-NAL-4-CHLORO-D-PHE-BETA-(3-PYRIDYL)-D-ALA-GLY-ARG-PRO-D-ALA-NH2(292141-31-2)
EPA Substance Registry System: AC-D-2-NAL-4-CHLORO-D-PHE-BETA-(3-PYRIDYL)-D-ALA-GLY-ARG-PRO-D-ALA-NH2(292141-31-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 292141-31-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 292141-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,1,4 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 292141-31:
(8*2)+(7*9)+(6*2)+(5*1)+(4*4)+(3*1)+(2*3)+(1*1)=122
122 % 10 = 2
So 292141-31-2 is a valid CAS Registry Number.

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292141-31-2Relevant academic research and scientific papers

Design and synthesis of potent hexapeptide and heptapeptide gonadotropin-releasing hormone antagonists by truncation of a decapeptide analogue sequence

Yahalom, Dror,Rahimipour, Shai,Koch, Yitzhak,Ben-Aroya, Nurit,Fridkin, Mati

, p. 2831 - 2836 (2007/10/03)

A novel strategy for designing reduced-size analogues of the decapeptide gonadotropin-releasing hormone (GnRH) was developed. As opposed to previous attempts to delete residues from either of the peptide's termini, our approach is based upon the known imp

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