Cas 388564-31-6,benzoic acid 17-(acetyl-prop-2-ynyl-amino)-16-hydroxymethyl-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1<i>H</i>-cyclopenta[<i>a</i>]phenanthren-3-yl ester

388564-31-6

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Basic information

Product Name: benzoic acid 17-(acetyl-prop-2-ynyl-amino)-16-hydroxymethyl-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester
Synonyms:
CAS NO:388564-31-6
Molecular Formula:
Molecular Weight: 501.666
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: benzoic acid 17-(acetyl-prop-2-ynyl-amino)-16-hydroxymethyl-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: benzoic acid 17-(acetyl-prop-2-ynyl-amino)-16-hydroxymethyl-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester(388564-31-6)
EPA Substance Registry System: benzoic acid 17-(acetyl-prop-2-ynyl-amino)-16-hydroxymethyl-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester(388564-31-6)

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: 388564-31-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 388564-31-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,8,5,6 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 388564-31:
(8*3)+(7*8)+(6*8)+(5*5)+(4*6)+(3*4)+(2*3)+(1*1)=196
196 % 10 = 6
So 388564-31-6 is a valid CAS Registry Number.

388564-31-6Upstream product

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388564-31-6Relevant academic research and scientific papers

An efficient synthesis of 1,4-oxazepines from β-formyl enamide using I2-NaHCO3 system

Longchar,Chetia,Ahmed,Boruah,Sandhu

, p. 3281 - 3287 (2001)

A new and efficient method for synthesis of 1,4-oxazepine has been developed utilizing I2-NaHCO3 promoted intramolecular cyclisation of N-progargyl-β-hydroxylmethyl enamide. The method is mild and simple.

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