Cas 121071-89-4,4-Nitro-benzoic acid (S)-3-iodo-2,2-dimethyl-1-((S)-4-methyl-2-oxo-cyclohex-3-enyl)-propyl ester

121071-89-4

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Basic information

Product Name: 4-Nitro-benzoic acid (S)-3-iodo-2,2-dimethyl-1-((S)-4-methyl-2-oxo-cyclohex-3-enyl)-propyl ester
Synonyms: 4-Nitro-benzoic acid (S)-3-iodo-2,2-dimethyl-1-((S)-4-methyl-2-oxo-cyclohex-3-enyl)-propyl ester
CAS NO:121071-89-4
Molecular Formula:
Molecular Weight: 471.292
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: 4-Nitro-benzoic acid (S)-3-iodo-2,2-dimethyl-1-((S)-4-methyl-2-oxo-cyclohex-3-enyl)-propyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-Nitro-benzoic acid (S)-3-iodo-2,2-dimethyl-1-((S)-4-methyl-2-oxo-cyclohex-3-enyl)-propyl ester(121071-89-4)
EPA Substance Registry System: 4-Nitro-benzoic acid (S)-3-iodo-2,2-dimethyl-1-((S)-4-methyl-2-oxo-cyclohex-3-enyl)-propyl ester(121071-89-4)

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: 121071-89-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 121071-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,0,7 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 121071-89:
(8*1)+(7*2)+(6*1)+(5*0)+(4*7)+(3*1)+(2*8)+(1*9)=84
84 % 10 = 4
So 121071-89-4 is a valid CAS Registry Number.

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121071-89-4Relevant academic research and scientific papers

DIASTEREOSELECTIVITY IN THE TiCl4-MEDIATED ALDOL REACTION OF CYCLIC DIENYLSILYL ETHERS

Barner, Bruce A.,Liu, Yalei,Rahman, Md. Abdur

, p. 6101 - 6112 (2007/10/02)

Cyclic dienylsilyl ethers derived from α,β-unsaturated ketones undergo TiCl4-catalyzed crossed aldol reactions with aldehydes, giving β'-hydroxy enone systems with good diastereoselectivity in most cases.The direction of stereocontrol (syn versus anti) in

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