Cas 1375414-70-2,N,N'-(tetrahydro-1H,1'H-6,6'-spirobi[pyrrolo[1,2-c]oxazol]-3,3'(5H,5'H)-diylidene)bis(4-methylbenzenesulfonamide)

1375414-70-2

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Basic information

Product Name: N,N'-(tetrahydro-1H,1'H-6,6'-spirobi[pyrrolo[1,2-c]oxazol]-3,3'(5H,5'H)-diylidene)bis(4-methylbenzenesulfonamide)
Synonyms:
CAS NO:1375414-70-2
Molecular Formula:
Molecular Weight: 544.653
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: N,N'-(tetrahydro-1H,1'H-6,6'-spirobi[pyrrolo[1,2-c]oxazol]-3,3'(5H,5'H)-diylidene)bis(4-methylbenzenesulfonamide)(CAS DataBase Reference)
NIST Chemistry Reference: N,N'-(tetrahydro-1H,1'H-6,6'-spirobi[pyrrolo[1,2-c]oxazol]-3,3'(5H,5'H)-diylidene)bis(4-methylbenzenesulfonamide)(1375414-70-2)
EPA Substance Registry System: N,N'-(tetrahydro-1H,1'H-6,6'-spirobi[pyrrolo[1,2-c]oxazol]-3,3'(5H,5'H)-diylidene)bis(4-methylbenzenesulfonamide)(1375414-70-2)

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: 1375414-70-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1375414-70-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,5,4,1 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1375414-70:
(9*1)+(8*3)+(7*7)+(6*5)+(5*4)+(4*1)+(3*4)+(2*7)+(1*0)=162
162 % 10 = 2
So 1375414-70-2 is a valid CAS Registry Number.

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1375414-70-2Relevant academic research and scientific papers

Highly stereoselective metal-free oxyaminations using chiral hypervalent iodine reagents

Farid, Umar,Wirth, Thomas

, p. 3462 - 3465 (2012/06/01)

The ring and I: Hypervalent iodine compounds avoid the issues of toxicity or complicated ligands of many transition-metal-based systems. A highly enantioselective oxyamination of alkenes with N-sulfonyl ureas employing chiral, lactic acid-based hypervalent iodine reagents gives a facile synthesis of enantiomerically pure 2-arylproline derivatives (see scheme) for the first time. Copyright

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