Cas 1224702-40-2,(3aR,5R,6S,6aR)-5-(benzylaminomethyl)-6-[(2-iodobenzyl)(tert-butoxycarbonyl)amino]-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxole

1224702-40-2

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Basic information

Product Name: (3aR,5R,6S,6aR)-5-(benzylaminomethyl)-6-[(2-iodobenzyl)(tert-butoxycarbonyl)amino]-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxole
Synonyms: (3aR,5R,6S,6aR)-5-(benzylaminomethyl)-6-[(2-iodobenzyl)(tert-butoxycarbonyl)amino]-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxole
CAS NO:1224702-40-2
Molecular Formula:
Molecular Weight: 594.49
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: (3aR,5R,6S,6aR)-5-(benzylaminomethyl)-6-[(2-iodobenzyl)(tert-butoxycarbonyl)amino]-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxole(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,5R,6S,6aR)-5-(benzylaminomethyl)-6-[(2-iodobenzyl)(tert-butoxycarbonyl)amino]-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxole(1224702-40-2)
EPA Substance Registry System: (3aR,5R,6S,6aR)-5-(benzylaminomethyl)-6-[(2-iodobenzyl)(tert-butoxycarbonyl)amino]-2,2-dimethyl-tetrahydrofuro[2,3-d][1,3]dioxole(1224702-40-2)

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: 1224702-40-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1224702-40-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,7,0 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1224702-40:
(9*1)+(8*2)+(7*2)+(6*4)+(5*7)+(4*0)+(3*2)+(2*4)+(1*0)=112
112 % 10 = 2
So 1224702-40-2 is a valid CAS Registry Number.

1224702-40-2Upstream product

1224702-40-2Downstream Products

1224702-52-6 (2R,3R,3aS,11aR)-10-benzyl-4-(tert-butoxycarbonyl)-2,3-(isopropylidenedioxy)-3a,4,5,10,11,11a-hexahydrofuro[3,2-b][1,5]benzodiazocine

1224702-40-2Relevant academic research and scientific papers

Palladium-catalyzed intramolecular aryl amination reaction: An expeditious approach to the synthesis of chiral benzodiazocine derivatives

Adhikary, Nirmal Das,Chattopadhyay, Partha

experimental part, p. 1754 - 1762 (2010/06/15)

A palladium-catalyzed method for intramolecular amination of aryl bromides and iodides has been developed employing different bulky biaryl phosphanes as ligands and toluene as solvent. A variety of electron-rich aryl halide substrates have been aminated b

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