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67627-99-0

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67627-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67627-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,2 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 67627-99:
(7*6)+(6*7)+(5*6)+(4*2)+(3*7)+(2*9)+(1*9)=170
170 % 10 = 0
So 67627-99-0 is a valid CAS Registry Number.

67627-99-0SDS

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 phenyl[(1-phenylmethyliden)-amino]acetic acid methyl ester

1.2 Other means of identification

Product number -
Other names N-benzyliden-α-phenyl-glycine methyl ester

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:67627-99-0 SDS

67627-99-0Relevant articles and documents

Straightforward and Highly Stereoselective Synthesis of 3,3,4-Trifluoropyrrolidines Involving 1,3-Dipolar Cycloaddition with 2,3,3-Trifluoroacrylate

Yamada, Shigeyuki,Higashi, Masao,Konno, Tsutomu,Ishihara, Takashi

, p. 4561 - 4568 (2016)

The reactions of benzyl 2,3,3-trifluoroacrylate with azomethine ylides, generated by the treatment of imino esters with lithium diisopropylamide, took place smoothly to give the corresponding 1,3-dipolar cycloadducts, fluorine-containing pyrrolidines, in good yields and with high diastereoselectivities (>95:5). When the fluorinated acrylate bore a chiral auxiliary as a substituent, for instance (l)-(–)-menthyl ester, the 1,3-dipolar cycloaddition reaction was found to give the corresponding fluorinated pyrrolidine derivatives in not only a diastereoselective but also an enantioselective manner.

Synthesis and Penicillin-binding Protein Inhibitory Assessment of Dipeptidic 4-Phenyl-β-lactams from α-Amino Acid-derived Imines

Decuyper, Lena,Juki?, Marko,Sosi?, Izidor,Amoroso, Ana Maria,Verlaine, Olivier,Joris, Bernard,Gobec, Stanislav,D'hooghe, Matthias

supporting information, p. 51 - 55 (2019/11/28)

Monocyclic β-lactams revive the research field on antibiotics, which are threatened by the emergence of resistant bacteria. A six-step synthetic route was developed, providing easy access to new 3-amino-1-carboxymethyl-4-phenyl-β-lactams, of which the penicillin-binding protein (PBP) inhibitory potency was demonstrated biochemically.

HETEROCYCLIC COMPOUNDS AS HIV PROTEASE INHIBITORS

-

Page/Page column 25, (2018/07/29)

The present invention is directed to compounds of Formula I, pharmaceutical compositions comprising the same, and their use in the inhibition of HIV protease, the inhibition of HIV replication, the prophylaxis of infection by HIV, the treatment of infection by HIV, and the prophylaxis, treatment, and delay in the onset or progression of AIDS.

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