Cas 1101861-75-9,(E)-N'-benzylidene-N-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl)methanesulfonohydrazide

1101861-75-9

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Basic information

Product Name: (E)-N'-benzylidene-N-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl)methanesulfonohydrazide
Synonyms: (E)-N'-benzylidene-N-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl)methanesulfonohydrazide
CAS NO:1101861-75-9
Molecular Formula:
Molecular Weight: 402.601
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: (E)-N'-benzylidene-N-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl)methanesulfonohydrazide(CAS DataBase Reference)
NIST Chemistry Reference: (E)-N'-benzylidene-N-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl)methanesulfonohydrazide(1101861-75-9)
EPA Substance Registry System: (E)-N'-benzylidene-N-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl)methanesulfonohydrazide(1101861-75-9)

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: 1101861-75-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1101861-75-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,1,8,6 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1101861-75:
(9*1)+(8*1)+(7*0)+(6*1)+(5*8)+(4*6)+(3*1)+(2*7)+(1*5)=109
109 % 10 = 9
So 1101861-75-9 is a valid CAS Registry Number.

1101861-75-9Upstream product

171628-52-7 C₈H₁₀N₂O₂S

1101861-75-9Downstream Products

1101861-75-9Relevant academic research and scientific papers

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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