Cas 256937-63-0,(S)-3-[4-[(5-iodo-4-pentenoyl)amino]phenoxy]-1-(isopropylamino)propan-2-ol

256937-63-0

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Basic information

Product Name: (S)-3-[4-[(5-iodo-4-pentenoyl)amino]phenoxy]-1-(isopropylamino)propan-2-ol
Synonyms: (S)-3-[4-[(5-iodo-4-pentenoyl)amino]phenoxy]-1-(isopropylamino)propan-2-ol
CAS NO:256937-63-0
Molecular Formula:
Molecular Weight: 432.302
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (S)-3-[4-[(5-iodo-4-pentenoyl)amino]phenoxy]-1-(isopropylamino)propan-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-[4-[(5-iodo-4-pentenoyl)amino]phenoxy]-1-(isopropylamino)propan-2-ol(256937-63-0)
EPA Substance Registry System: (S)-3-[4-[(5-iodo-4-pentenoyl)amino]phenoxy]-1-(isopropylamino)propan-2-ol(256937-63-0)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 256937-63-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 256937-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,9,3 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 256937-63:
(8*2)+(7*5)+(6*6)+(5*9)+(4*3)+(3*7)+(2*6)+(1*3)=180
180 % 10 = 0
So 256937-63-0 is a valid CAS Registry Number.

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256937-63-0Relevant academic research and scientific papers

Synthesis of an iodine-labelled analogue of practolol: (S)-3-[4-(4-iodobut-3-encarboxamido)phenoxy]-1-isopropylaminoepropan-2-ol (AMI-9S)

Apparu, Marcel,Ben Tiba, Younes,Leo, Pierre-Marc,Mathieu, Jean Paul,Mauclaire, Laurent

, p. 1195 - 1202 (1999)

AMI-9S was synthesized in the S configuration with an enantiomeric purity of over 97% and labelled with iodine-123 with a specific activity of 300 Ci/mmol. Enantiomeric purity was determined by 19F NMR spectroscopy following derivatisation usin

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