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75154-68-6

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75154-68-6 Usage

Chemical Properties

Off-White Solid

Uses

Methyl (S)-N-Tritylaziridine-2-carboxylate (cas# 75154-68-6) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 75154-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,5 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75154-68:
(7*7)+(6*5)+(5*1)+(4*5)+(3*4)+(2*6)+(1*8)=136
136 % 10 = 6
So 75154-68-6 is a valid CAS Registry Number.
InChI:InChI=1/C23H21NO2/c1-26-22(25)21-17-24(21)23(18-11-5-2-6-12-18,19-13-7-3-8-14-19)20-15-9-4-10-16-20/h2-16,21H,17H2,1H3/t21-,24?/m0/s1

75154-68-6 Well-known Company Product Price

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  • Aldrich

  • (516015)  Methyl(S)-(−)-1-tritylaziridine-2-carboxylate  98%

  • 75154-68-6

  • 516015-5G

  • 969.93CNY

  • Detail

75154-68-6SDS

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 Methyl (S)-N-Tritylaziridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names methyl (2S)-1-tritylaziridine-2-carboxylate

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:75154-68-6 SDS

75154-68-6Relevant articles and documents

Synthesis and Stability of the Cyclic Sulfamidate of N-Trityl-L-Serine Methyl Ester

Pilkington, Melanie,Wallis, John D.

, p. 1857 - 1858 (1993)

The title compound 12, prepared in three steps from L-serine methyl ester, is thermally stable 50 deg C; the formation of the cyclic sulfamidite 9, rather than acyclic products, in the reaction of thionyl chloride with vic-amino alcohol 7 is far more de

Straightforward synthesis and antioxidant studies of chalcogenoaziridines

Borges, Rodrigo,Andrade, Floyd C.D.,Schwab, Ricardo S.,Sousa, Fernanda S.S.,de Souza, Maurice Neto,Savegnago, Lucielli,Schneider, Paulo H.

supporting information, p. 3501 - 3504 (2016/07/15)

Herein we reported the synthesis of chalcogenoaziridines through the introduction of the organoselenium moiety in the aziridine framework through the nucleophilic substitution of the OTs leaving group. In addition, the antioxidant activity, as reflected b

Total synthesis and activity of the metallo-β-lactamase inhibitor aspergillomarasmine A

Koteva, Kalinka,King, Andrew M.,Capretta, Alfredo,Wright, Gerard D.

supporting information, p. 2210 - 2212 (2016/02/19)

Resistance to β-lactam antibiotics is mediated primarily by enzymes that hydrolytically inactivate the drugs by one of two mechanisms: serine nucleophilic attack or metal-dependent activation of a water molecule. Serine β-lactamases are countered in the c

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