Cas 351011-92-2,2-tert-butyldimethylsilyl-5-[(1'R,3'S)-3'-dibenzylamino-1',4'-dihydroxybutyl]-N,N-dimethylimidazole-1-sulfonamide

351011-92-2

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Basic information

Product Name: 2-tert-butyldimethylsilyl-5-[(1'R,3'S)-3'-dibenzylamino-1',4'-dihydroxybutyl]-N,N-dimethylimidazole-1-sulfonamide
Synonyms: 2-tert-butyldimethylsilyl-5-[(1'R,3'S)-3'-dibenzylamino-1',4'-dihydroxybutyl]-N,N-dimethylimidazole-1-sulfonamide
CAS NO:351011-92-2
Molecular Formula:
Molecular Weight: 572.844
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: 2-tert-butyldimethylsilyl-5-[(1'R,3'S)-3'-dibenzylamino-1',4'-dihydroxybutyl]-N,N-dimethylimidazole-1-sulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-tert-butyldimethylsilyl-5-[(1'R,3'S)-3'-dibenzylamino-1',4'-dihydroxybutyl]-N,N-dimethylimidazole-1-sulfonamide(351011-92-2)
EPA Substance Registry System: 2-tert-butyldimethylsilyl-5-[(1'R,3'S)-3'-dibenzylamino-1',4'-dihydroxybutyl]-N,N-dimethylimidazole-1-sulfonamide(351011-92-2)

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: 351011-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 351011-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,0,1 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 351011-92:
(8*3)+(7*5)+(6*1)+(5*0)+(4*1)+(3*1)+(2*9)+(1*2)=92
92 % 10 = 2
So 351011-92-2 is a valid CAS Registry Number.

351011-92-2Upstream product

351011-92-2Downstream Products

351011-92-2Relevant academic research and scientific papers

Synthesis of CIS- or trans-2,4-disubstituted tetrahydrofurans bearing amino and imidazole groups by efficient use of the modified or standard mitsunobu cyclization: Synthetic studies toward novel histamine H3-ligands

Araki, Lisa,Harusawa, Shinya,Ijichi, Ikuno,Ohishi, Hirofumi,Kurihara, Takushi

, p. 889 - 903 (2007/10/03)

4(5)-[(2R,4S) or (2S,4S)-4-Aminotetrahydrofuran-2-yl]imidazole [(-)-1a or (-)-1b] and its enantiomers [(+)-2a and (+)-2b] were synthesized by efficient use of the modified or standard Mitsunobu cyclization.

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