Cas 930599-20-5,N-isopropylidene-N'-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-N'-2-nitrobenzenesulfonyl hydrazide

930599-20-5

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Basic information

Product Name: N-isopropylidene-N'-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-N'-2-nitrobenzenesulfonyl hydrazide
Synonyms: N-isopropylidene-N'-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-N'-2-nitrobenzenesulfonyl hydrazide
CAS NO:930599-20-5
Molecular Formula:
Molecular Weight: 461.626
EINECS: N/A
Product Categories: N/A
Mol File: 930599-20-5.mol
Article Data: 2

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-isopropylidene-N'-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-N'-2-nitrobenzenesulfonyl hydrazide(CAS DataBase Reference)
NIST Chemistry Reference: N-isopropylidene-N'-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-N'-2-nitrobenzenesulfonyl hydrazide(930599-20-5)
EPA Substance Registry System: N-isopropylidene-N'-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-N'-2-nitrobenzenesulfonyl hydrazide(930599-20-5)

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: 930599-20-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 930599-20-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,0,5,9 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 930599-20:
(8*9)+(7*3)+(6*0)+(5*5)+(4*9)+(3*9)+(2*2)+(1*0)=185
185 % 10 = 5
So 930599-20-5 is a valid CAS Registry Number.

930599-20-5Upstream product

930599-20-5Downstream Products

930599-20-5Relevant articles and documents

A stereospecific palladium-catalyzed route to monoalkyl diazenes for mild allylic reduction

Movassaghi, Mohammad,Ahmad, Omar K.

supporting information; experimental part, p. 8909 - 8912 (2009/05/26)

(Chemical Equation Presented) One step beyond: The first single-step stereospecific transition-metal-catalyzed conversion of allylic electrophiles into monoalkyl diazenes is described. This synthesis of allylic monoalkyl diazenes offers a new strategy for asymmetric synthesis by the reduction of optically active substrates or the use of chiral catalyst systems. Sensitive substrates are reduced in a highly selective manner. Ar = 2-NO2C 6H2.

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