Cas 1092807-33-4,(S)-5-[bis(3,5-dimethylphenyl)(hydroxy)methyl]-2-phenyl-6,7-dihydro-5H-pyrrolo[2,1-c]-1,2,4-triazol-2-ium tetrafluoroborate

1092807-33-4

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Basic information

Product Name: (S)-5-[bis(3,5-dimethylphenyl)(hydroxy)methyl]-2-phenyl-6,7-dihydro-5H-pyrrolo[2,1-c]-1,2,4-triazol-2-ium tetrafluoroborate
Synonyms: (S)-5-[bis(3,5-dimethylphenyl)(hydroxy)methyl]-2-phenyl-6,7-dihydro-5H-pyrrolo[2,1-c]-1,2,4-triazol-2-ium tetrafluoroborate
CAS NO:1092807-33-4
Molecular Formula:
Molecular Weight: 511.37
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: (S)-5-[bis(3,5-dimethylphenyl)(hydroxy)methyl]-2-phenyl-6,7-dihydro-5H-pyrrolo[2,1-c]-1,2,4-triazol-2-ium tetrafluoroborate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-5-[bis(3,5-dimethylphenyl)(hydroxy)methyl]-2-phenyl-6,7-dihydro-5H-pyrrolo[2,1-c]-1,2,4-triazol-2-ium tetrafluoroborate(1092807-33-4)
EPA Substance Registry System: (S)-5-[bis(3,5-dimethylphenyl)(hydroxy)methyl]-2-phenyl-6,7-dihydro-5H-pyrrolo[2,1-c]-1,2,4-triazol-2-ium tetrafluoroborate(1092807-33-4)

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: 1092807-33-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1092807-33-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,8,0 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1092807-33:
(9*1)+(8*0)+(7*9)+(6*2)+(5*8)+(4*0)+(3*7)+(2*3)+(1*3)=154
154 % 10 = 4
So 1092807-33-4 is a valid CAS Registry Number.

1092807-33-4Upstream product

1092807-27-6 (S)-5-[bis(3,5-dimethylphenyl)(trimethylsiloxy)methyl]-2-phenyl-6,7-dihydro-5H-pyrrolo[2,1-c]-1,2,4-triazol-2-ium tetrafluoroborate

1092807-33-4Downstream Products

1092807-33-4Relevant academic research and scientific papers

Chiral bifunctional n-heterocyclic carbenes: Synthesis and application in the aza-Morita-Baylis-Hillman reaction

He, Lin,Zhang, Yan-Rong,Huang, Xue-Liang,Ye, Song

, p. 2825 - 2829 (2008)

A series of chiral bifunctional N-heterocyclic carbene (NHC) precursors with a proximal hydroxy group were smoothly prepared from L-pyroglutamic acid. Promising enantiomeric excesses (up to 44% ee) were achieved for the bifunctional NHC-catalyzed enantioselective aza-Morita-Baylis-Hillman reaction of cyclopent-2-enone with N-tosylphenylmethanimine. Georg Thieme Verlag Stuttgart.

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