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Carbamic acid, [2-[1-[(4-methylphenyl)sulfonyl]-1H-indol-3-yl]ethyl]-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

727416-67-3

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727416-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 727416-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,7,4,1 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 727416-67:
(8*7)+(7*2)+(6*7)+(5*4)+(4*1)+(3*6)+(2*6)+(1*7)=173
173 % 10 = 3
So 727416-67-3 is a valid CAS Registry Number.

727416-67-3SDS

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 3-[2-{N-(tert-butoxycarbonyl)amino}ethyl]-1-(p-toluenesulfonyl)indole

1.2 Other means of identification

Product number -
Other names 3-[2-(tert-butoxycarbonylamino)ethyl]-N-(p-toluenesulfonyl)indole

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:727416-67-3 SDS

727416-67-3Downstream Products

727416-67-3Relevant academic research and scientific papers

Access to Indole-Fused Benzannulated Medium-Sized Rings through a Gold(I)-Catalyzed Cascade Cyclization of Azido-Alkynes

Greiner, Luca C.,Inuki, Shinsuke,Arichi, Norihito,Oishi, Shinya,Suzuki, Rikito,Iwai, Tomohiro,Sawamura, Masaya,Hashmi, A. Stephen K.,Ohno, Hiroaki

, p. 12992 - 12997 (2021/07/20)

Because benzannulated and indole-fused medium-sized rings are found in many bioactive compounds, combining these fragments might lead to unexplored areas of biologically relevant and uncovered chemical space. Herein is shown that α-imino gold carbene chem

[TPA][Pro] ionic liquid as efficient reaction medium for N-tert-Boc protection of amines

Vijaya Durga,Rambabu,Srinivasa Reddy,Hari Babu

, p. 1313 - 1316 (2017/05/02)

A facile and efficient N-tert-Boc protection of amines is described by the reaction of various primary, secondary, benzylic and aryl amines with di-tert-butyl dicarbonate in the ionic liquid [TPA][Pro] at room temperature. All the N-tert-butylcarbamates are afforded in excellent yields. A catalyst-free method was developed and the ionic liquid [TPA][Pro] can be recovered and reused for several times without loss of its activity.

An environmentally friendly protocol for oxidative halocyclization of tryptamine and tryptophol derivatives

Xu, Jun,Tong, Rongbiao

, p. 2952 - 2956 (2017/07/24)

An environmentally friendly and efficient protocol (KX/oxone) for oxidative halocyclization of tryptamine/tryptophol derivatives was developed and demonstrated with 28 examples and concise total synthesis of cyclotryptamine alkaloid protubonines A and B. The distinct advantage of this protocol over all previous methods is that no organic byproduct is generated from a halogenating agent or oxidant, thus greatly reducing the environmental impact of halocyclization and facilitating the post-reaction purification.

Facile N-tert-butoxycarbonylation of amines using La(NO3)3·6H2O as a mild and efficient catalyst under solvent-free conditions

Suryakiran,Prabhakar,Reddy, T. Srikanth,Rajesh,Venkateswarlu

, p. 8039 - 8042 (2007/10/03)

Facile N-tert-butoxycarbonylation of amines is described by the treatment of various primary, secondary, benzylic and aryl amines with di-tert-butyl dicarbonate in the presence of catalytic amounts of La(NO3)3·6H2O under solvent-free conditions at room temperature to afford N-tert-butylcarbamates in excellent yields.

Catalytic asymmetric hydrogenation of indoles using a rhodium complex with a chiral bisphosphine ligand PhTRAP

Kuwano, Ryoichi,Kashiwabara, Manabu,Sato, Koji,Ito, Takashi,Kaneda, Kohei,Ito, Yoshihiko

, p. 521 - 535 (2007/10/03)

Highly enantioselective hydrogenation of N-protected indoles was successfully developed by use of the rhodium catalyst generated in situ from [Rh(nbd)2]SbF6 and the chiral bisphosphine PhTRAP, which can form a trans-chelate complex with a transition metal atom. The PhTRAP-rhodium catalyst required a base (e.g., Cs2CO3) for the achievement of high enantioselectivity. Various 2-substituted N-acetylindoles were converted into the corresponding chiral indolines with up to 95% ee. The hydrogenations of 3-substituted N-tosylindoles yielded indolines possessing a stereogenic center at the 3-position with high enantiomeric excesses (up to 98% ee).

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