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Heptanoic acid, 2-[2-oxo-2-[(phenylmethoxy)(phenylmethyl)amino]ethyl]-, 1,1-dimethylethyl ester, (2R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122501-60-4

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122501-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122501-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,5,0 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 122501-60:
(8*1)+(7*2)+(6*2)+(5*5)+(4*0)+(3*1)+(2*6)+(1*0)=74
74 % 10 = 4
So 122501-60-4 is a valid CAS Registry Number.

122501-60-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-(+)-tert-Butyl 2-(N-benzyl-N-benzyloxycarbamoylmethyl)heptanoate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:122501-60-4 SDS

122501-60-4Relevant academic research and scientific papers

Asymmetric Synthesis of (-)-Actinonin and (-)-epi-Actinonin

Bashiardes, George,Bodwell, Graham J.,Davies, Stephen G.

, p. 459 - 470 (2007/10/02)

The highly asymmetric induction imparted by the iron chiral auxiliary 5-C5H5)Fe(CO)(PPh3)> is exploited in the preparation of homochiral (R)- and (S)-α-pentylsuccinates.Their application in the synthesis of (-)-actinonin and (-)-epi-actinoni

THE ASYMMETRIC SYNTHESIS OF (-)-ACTINONIN USING THE IRON CHIRAL AUXILIARY 5-C5H5)Fe(CO)(PPh3)>

Bashiardes, George,Davies, Stephen G.

, p. 6509 - 6512 (2007/10/02)

The asymmetric synthesis of the α-pentyl succinate fragment of (-)-Actinonin is achived using the chiral ironacetyl S-(+)-5-C5H5)-Fe(CO)(PPh3)COCH3> and subsequently converted to (-)-Actinonin in an overall yield of 41percent.

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