Cas 122913-35-3,(+/-)-(2S<sup>*</sup>,3S<sup>*</sup>)-2-(2'-phenylethyl)-3-(3''-iodopropyl)succinimide

122913-35-3

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Basic information

Product Name: (+/-)-(2S^*,3S^*)-2-(2'-phenylethyl)-3-(3''-iodopropyl)succinimide
Synonyms: (+/-)-(2S^*,3S^*)-2-(2'-phenylethyl)-3-(3''-iodopropyl)succinimide
CAS NO:122913-35-3
Molecular Formula:
Molecular Weight: 371.218
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: (+/-)-(2S^*,3S^*)-2-(2'-phenylethyl)-3-(3''-iodopropyl)succinimide(CAS DataBase Reference)
NIST Chemistry Reference: (+/-)-(2S^*,3S^*)-2-(2'-phenylethyl)-3-(3''-iodopropyl)succinimide(122913-35-3)
EPA Substance Registry System: (+/-)-(2S^*,3S^*)-2-(2'-phenylethyl)-3-(3''-iodopropyl)succinimide(122913-35-3)

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: 122913-35-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 122913-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,9,1 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 122913-35:
(8*1)+(7*2)+(6*2)+(5*9)+(4*1)+(3*3)+(2*3)+(1*5)=103
103 % 10 = 3
So 122913-35-3 is a valid CAS Registry Number.

122913-35-3Upstream product

122913-35-3Downstream Products

122913-35-3Relevant academic research and scientific papers

HYPERVALENT ORGANOIODINE REAGENTS IN THE β-FRAGMENTATION OF BICYCLIC CARBINOLAMIDES LEADING TO IMIDES

Hernandez, R.,Marrero, J. J.,Melian, D.,Suarez, E.

, p. 6661 - 6664 (1988)

A mild and convenient method for the synthesis of 3,4-substituted cyclic imides by photolysis of bicyclic - and -carbinolamides in the presence of (diacetoxyiodo)-benzene and iodine is described.

RADICAL β-FRAGMENTATION OF BICYCLOCARBINOLAMIDES: SYNTHESIS OF FIVE- AND EIGHT-MEMBERED CYCLIC IMIDES

Hernandez, Rosendo,Melian, Daniel,Prange, Thierry,Suarez, Ernesto

, p. 439 - 454 (2007/10/02)

The influence of 4-alkyl or 4-aryl substituents in the regioselectivity of the β-fragmentation of carbinolamidyl radicals generated from the corresponding carbinolamides (7-13) by irradiation with visible light in the presence of (diacetoxyiodo)benzene an

A Selenurane Derivative Promotes β-Fragmentation of Carbinolamides Leading to Cyclic Imides

Dorta, Rosa L.,Francisco, Cosme G.,Suarez, Ernesto

, p. 1083 - 1086 (2007/10/02)

The alkoxy radical intermediates generated by reaction of carbinolamides with diphenylselenium hydroxyacetate (1) in the presence of iodine and under irradiation with visible light undergo β-fragmentation to afford 3,4-substituted cyclic imides in good yields.

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