Cas 851935-64-3,{2-[(4,5-dimethoxy-2-nitro-phenyl)-(2-hydroxy-6-oxo-cyclohex-1-enyl)-methylsulfanyl]-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester

851935-64-3

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Basic information

Product Name: {2-[(4,5-dimethoxy-2-nitro-phenyl)-(2-hydroxy-6-oxo-cyclohex-1-enyl)-methylsulfanyl]-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester
Synonyms: {2-[(4,5-dimethoxy-2-nitro-phenyl)-(2-hydroxy-6-oxo-cyclohex-1-enyl)-methylsulfanyl]-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester
CAS NO:851935-64-3
Molecular Formula:
Molecular Weight: 604.681
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-[(4,5-dimethoxy-2-nitro-phenyl)-(2-hydroxy-6-oxo-cyclohex-1-enyl)-methylsulfanyl]-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {2-[(4,5-dimethoxy-2-nitro-phenyl)-(2-hydroxy-6-oxo-cyclohex-1-enyl)-methylsulfanyl]-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester(851935-64-3)
EPA Substance Registry System: {2-[(4,5-dimethoxy-2-nitro-phenyl)-(2-hydroxy-6-oxo-cyclohex-1-enyl)-methylsulfanyl]-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester(851935-64-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 851935-64-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 851935-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,9,3 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 851935-64:
(8*8)+(7*5)+(6*1)+(5*9)+(4*3)+(3*5)+(2*6)+(1*4)=193
193 % 10 = 3
So 851935-64-3 is a valid CAS Registry Number.

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851935-64-3Relevant academic research and scientific papers

A three-component photoreversible tag for thiols

Clarke, Kristine M.,La Clair, James J.,Burkart, Michael D.

, p. 3709 - 3711 (2007/10/03)

(Chemical Equation Presented) A one-pot coupling of a 1,3-diketone, an aldehyde, and an alkanethiol has been developed to produce a protected sulfide. Through use of an o-nitrophenylbenzaldehyde, this method provides a one-step route to a photochemically reversible thiol-protecting group. The kinetics of photolysis were established using 1H NMR analysis, which allows for the rate to be based on the entire reaction scheme.

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