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335254-69-8

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335254-69-8 Usage

General Description

Tert-butyl (4-iodo-2-nitrophenyl)carbamate is a chemical compound with the molecular formula C13H16IN2O4. It is a carbamate derivative containing a tert-butyl group attached to a 4-iodo-2-nitrophenyl group. tert-butyl (4-iodo-2-nitrophenyl)carbaMate is commonly used in organic synthesis as a building block for the preparation of various pharmaceuticals and agrochemicals. It is often employed as a reagent in the synthesis of biologically active compounds due to its versatility and stability. Tert-butyl (4-iodo-2-nitrophenyl)carbamate may also have potential applications in materials science and chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 335254-69-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,5,2,5 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 335254-69:
(8*3)+(7*3)+(6*5)+(5*2)+(4*5)+(3*4)+(2*6)+(1*9)=138
138 % 10 = 8
So 335254-69-8 is a valid CAS Registry Number.

335254-69-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-(4-iodo-2-nitrophenyl)carbamate

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:335254-69-8 SDS

335254-69-8Relevant articles and documents

New class of bioluminogenic probe based on bioluminescent enzyme-induced electron transfer: BioLeT

Takakura, Hideo,Kojima, Ryosuke,Kamiya, Mako,Kobayashi, Eiji,Komatsu, Toru,Ueno, Tasuku,Terai, Takuya,Hanaoka, Kenjiro,Nagano, Tetsuo,Urano, Yasuteru

supporting information, p. 4010 - 4013 (2015/04/14)

Bioluminescence imaging (BLI) has advantages for investigating biological phenomena in deep tissues of living animals, but few design strategies are available for functional bioluminescent substrates. We propose a new design strategy (designated as bioluminescent enzyme-induced electron transfer: BioLeT) for luciferin-based bioluminescence probes. Luminescence measurements of a series of aminoluciferin derivatives confirmed that bioluminescence can be controlled by means of BioLeT. Based on this concept, we developed bioluminescence probes for nitric oxide that enabled quantitative and sensitive detection even in vivo. Our design strategy should be applicable to develop a wide range of practically useful bioluminogenic probes.

NOVEL BENZODIAZEPINONES AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTOR FUNCTIONS AND NEUROLOGICAL USES THEREOF

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Paragraph 0124; 0125; 0128, (2013/03/28)

The present invention relates to novel benzodiazepinone compounds of Formulae (I) wherein R1, R2, R4, R6, R7, R8, R9, and R10 are as defined herein. The invention also

Glutamate receptor antagonists

-

, (2008/06/13)

The present invention relates to compounds of with a base structure of formula 1 The compounds of formula I are shown to have activity as metabotropic glutamate receptor antagonists.

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