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128018-18-8

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128018-18-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128018-18-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,0,1 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 128018-18:
(8*1)+(7*2)+(6*8)+(5*0)+(4*1)+(3*8)+(2*1)+(1*8)=108
108 % 10 = 8
So 128018-18-8 is a valid CAS Registry Number.

128018-18-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Pyrrolidinecarboxamide,N-(1,1-dimethylethyl)-,(2S)-(9CI)

1.2 Other means of identification

Product number -
Other names H-PROLINE-TERT-BUTYL AMIDE

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:128018-18-8 SDS

128018-18-8Relevant articles and documents

KNI-102, a novel tripeptide HIV protease inhibitor containing allophenylnorstatine as a transition-state mimic

Mimoto,Imai,Tanaka,Hattori,Kisanuki,Akaji,Kiso

, p. 3088 - 3088 (1991)

HIV-1 protease inhibitors containing allophenylnorstatine (Apns; (2S,3S)-3-amino-2-hydroxy-4-phenyl-butyric acid]-Pro (syn distereomer) as a transition-state mimic were established to be potent and highly selective. Z-Asn-Apns-Pro-NHBu(t) (KNI-102) is the only tripeptide exhibiting substantial anti-HIV activity and may be of minimum size for potent, selective inhibition of HIV protease. Ready availability due to its simple chemical structure and stability should make it valuable for studies of the development of metabolically stable anti-AIDS drugs.

The development of new amine-amide ligands for application in Cu(II)-catalyzed enantioselective Henry reactions

Ao, Chunyan,Men, Jian,Wang, Yang,Shao, Tao,Huang, Yuanyuan,Huo, Junji,Gao, Guowei

, p. 589 - 595 (2016/07/06)

A new type of chiral tertiary amine ligand was designed and derived from l-proline and (R)-BINOL. These new chiral ligands chelated with Cu(II) showed highly catalytic efficiency in enantioselective Henry reactions. Excellent yields (up to 99%) and high enantioselectivities (up to 96% ee) were achieved for aromatic, hetero-aromatic and aliphatic aldehyde substrates, without an additional base additive or the need for air or moisture exclusion.

Stereoselective synthesis of 5-substituted pyrrolo[1,2-c]imidazol-3-ones: Access to annulated chiral imidazol(in)ium salts

Metallinos, Costa,Xu, Shufen

supporting information; experimental part, p. 76 - 79 (2010/03/03)

"Chemical Equation Presented" A two-step synthesis of N-heterocyclic carbene (NHC) precatalysts by diastereoselective or enantioselective lithiation of pyrrolo[1,2-c]imidazol-3-ones followed by POCl3-induced salt formation is described. The res

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