Cas 890653-19-7,N<sub>1</sub>,N<sub>6</sub>-bis[(1S,2R)-2-(tert-butyl-dimethyl-silanyloxy)-indan-1-yl]-(2R,3R,4R,5R)-2,5-bis(iodobenzyloxy)-3,4-dihydroxyhexane-1,6-diamide

890653-19-7

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Basic information

Product Name: N₁,N₆-bis[(1S,2R)-2-(tert-butyl-dimethyl-silanyloxy)-indan-1-yl]-(2R,3R,4R,5R)-2,5-bis(iodobenzyloxy)-3,4-dihydroxyhexane-1,6-diamide
Synonyms: N₁,N₆-bis[(1S,2R)-2-(tert-butyl-dimethyl-silanyloxy)-indan-1-yl]-(2R,3R,4R,5R)-2,5-bis(iodobenzyloxy)-3,4-dihydroxyhexane-1,6-diamide
CAS NO:890653-19-7
Molecular Formula:
Molecular Weight: 1133.06
EINECS: N/A
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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: N₁,N₆-bis[(1S,2R)-2-(tert-butyl-dimethyl-silanyloxy)-indan-1-yl]-(2R,3R,4R,5R)-2,5-bis(iodobenzyloxy)-3,4-dihydroxyhexane-1,6-diamide(CAS DataBase Reference)
NIST Chemistry Reference: N₁,N₆-bis[(1S,2R)-2-(tert-butyl-dimethyl-silanyloxy)-indan-1-yl]-(2R,3R,4R,5R)-2,5-bis(iodobenzyloxy)-3,4-dihydroxyhexane-1,6-diamide(890653-19-7)
EPA Substance Registry System: N₁,N₆-bis[(1S,2R)-2-(tert-butyl-dimethyl-silanyloxy)-indan-1-yl]-(2R,3R,4R,5R)-2,5-bis(iodobenzyloxy)-3,4-dihydroxyhexane-1,6-diamide(890653-19-7)

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Hazard Codes: N/A
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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 890653-19-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 890653-19-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,0,6,5 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 890653-19:
(8*8)+(7*9)+(6*0)+(5*6)+(4*5)+(3*3)+(2*1)+(1*9)=197
197 % 10 = 7
So 890653-19-7 is a valid CAS Registry Number.

890653-19-7Upstream product

890653-19-7Downstream Products

890653-21-1 N₁,N₆-bis[(1S,2R)-2-(tert-butyl-dimethyl-silanyloxy)-indan-1-yl]-(2R,3R,4R,5R)-2,5-bis(2-carbamoylbenzyloxy)-3,4-dihydroxyhexane-1,6-diamine

890653-19-7Relevant academic research and scientific papers

Hydroxylamine as an ammonia equivalent in microwave-enhanced aminocarbonylations

Wu, Xiongyu,Wannberg, Johan,Larhed, Mats

, p. 4665 - 4670 (2006)

A novel palladium-catalyzed and Mo(CO)6 promoted aminocarbonylation protocol was developed for rapid generation of primary aromatic amides from aryl bromides and iodides. Employing controlled microwave heating, hydroxylamine was first reduced in situ to ammonia, which thereafter reacted with carbon monoxide and the aryl halide substrate, delivering the benzamide product in less than 20 min. Based on this in situ carbonylation, a facile preparation of a novel HIV-1 protease inhibitor was achieved.

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