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Carbamic acid, (4-nitropentyl)(phenylmethyl)-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

448957-40-2

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448957-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 448957-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,8,9,5 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 448957-40:
(8*4)+(7*4)+(6*8)+(5*9)+(4*5)+(3*7)+(2*4)+(1*0)=202
202 % 10 = 2
So 448957-40-2 is a valid CAS Registry Number.

448957-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[N-benzyl-(N-tert-butyloxycarbonyl)]amino-2-nitropentane

1.2 Other means of identification

Product number -
Other names 5-[N-benzyl-N-(tert-butyloxycarbonyl)]amino-2-nitropentane

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:448957-40-2 SDS

448957-40-2Relevant academic research and scientific papers

Tandem polar/radical crossover sequences for the formation of fused and bridged bicyclic nitrogen heterocycles involving radical ionic chain reactions, and alkene radical cation intermediates, performed under reducing conditions: Scope and limitations

Crich, David,Ranganathan, Krishnakumar,Neelamkavil, Santhosh,Huang, Xianhai

, p. 7942 - 7947 (2007/10/03)

It is demonstrated that phosphorylated forms of β-nitro alcohols provide an excellent means of entry into β-(phosphatoxy)alkyl radicals on exposure to tributyltin hydride and AIBN in benzene at reflux. These radicals then undergo heterolytic cleavage of t

Generation and trapping of alkene radical cations under nonoxidizing conditions: Formation of six-membered rings by exo- and endo-mode cyclizations

Crich, David,Neelamkavil, Santhosh

, p. 2573 - 2575 (2007/10/03)

(Matrix presented) It is demonstrated that alkene radical cations generated by the radical ionic fragmentation of β-(phosphatoxy)alkyl radicals undergo efficient nucleophilic capture by amines in either the 6-exo or 6-endo modes, leading to six-membered n

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