Cas 1214750-35-2,(S)-5-bromo-3-(4-(diethylamino)-2-hydroxyphenyl)-3-hydroxy-1-methylindol-2-one

1214750-35-2

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Basic information

Product Name: (S)-5-bromo-3-(4-(diethylamino)-2-hydroxyphenyl)-3-hydroxy-1-methylindol-2-one
Synonyms:
CAS NO:1214750-35-2
Molecular Formula:
Molecular Weight: 405.291
EINECS: N/A
Product Categories: N/A
Mol File: 1214750-35-2.mol
Article Data: 1

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)-5-bromo-3-(4-(diethylamino)-2-hydroxyphenyl)-3-hydroxy-1-methylindol-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (S)-5-bromo-3-(4-(diethylamino)-2-hydroxyphenyl)-3-hydroxy-1-methylindol-2-one(1214750-35-2)
EPA Substance Registry System: (S)-5-bromo-3-(4-(diethylamino)-2-hydroxyphenyl)-3-hydroxy-1-methylindol-2-one(1214750-35-2)

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: 1214750-35-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1214750-35-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,7,5 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1214750-35:
(9*1)+(8*2)+(7*1)+(6*4)+(5*7)+(4*5)+(3*0)+(2*3)+(1*5)=122
122 % 10 = 2
So 1214750-35-2 is a valid CAS Registry Number.

1214750-35-2Upstream product

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1214750-35-2Relevant articles and documents

Catalytic asymmetric synthesis of substituted 3-hydroxy-2oxindoles

Hanhan, Nadine V.,Sahin, Aziza H.,Chang, Toby W.,Fettinger, James C.,Franz, Annaliese K.

supporting information; experimental part, p. 744 - 747 (2010/04/06)

Chemical equation presented Chemical equation presented No more double trouble: The competing double-addition pathway was suppressed when chiral scandium(III) and indium (III) complexes were used to catalyze the addition of indoles and other π nucleophile

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