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67877-95-6

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67877-95-6 Usage

General Description

(S)-4-Nitrophenylalanine methyl ester hydrochloride is a chemical compound that is derived from the essential amino acid phenylalanine. It is a methyl ester of 4-nitrophenylalanine and is typically found in a crystalline form. (S)-4-NITROPHENYLALANINE METHYL ESTER HYDROCHLORIDE is primarily used in chemical research and as a building block for the synthesis of other compounds. It is also used as a chiral catalyst and in the production of pharmaceuticals. The hydrochloride form of this compound is a salt that is more soluble in water, making it easier to handle and work with in laboratory settings. Overall, (S)-4-Nitrophenylalanine methyl ester hydrochloride is an important chemical with various applications in the fields of chemistry and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 67877-95-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,7 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 67877-95:
(7*6)+(6*7)+(5*8)+(4*7)+(3*7)+(2*9)+(1*5)=196
196 % 10 = 6
So 67877-95-6 is a valid CAS Registry Number.

67877-95-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-4-NITROPHENYLALANINE METHYL ESTER HYDROCHLORIDE

1.2 Other means of identification

Product number -
Other names H-p-Nitro-D-Phe-OMe

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:67877-95-6 SDS

67877-95-6Relevant articles and documents

AMINO ACID DERIVATIVES AND ABSORBABLE POLYMERS THEREFROM

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Paragraph 0243; 0244, (2016/09/26)

The present invention relates to the discovery of new class of hydrolysable amino acid derivatives and absorbable polyester amides, polyamides, polyepoxides, polyureas and polyurethanes prepared therefrom. The resultant absorbable polymers are useful for drug delivery, tissue engineering, tissue adhesives, adhesion prevention, bone wax formulations, medical device coatings, stents, stent coatings, highly porous foams, reticulated foams, wound care, cardiovascular applications, orthopedic devices, surface modifying agents and other implantable medical devices. In addition, these absorbable polymers should have a controlled degradation profile.

Synthesis and bioactivity of novel 3-(1-hydroxyethylidene)-5-substituted- pyrrolidine-2,4-dione derivatives

Han, Bao Feng,Shi, Qing Ming,Wang, Xian Feng,Liu, Jian Bo,Qiang, Sheng,Yang, Chun Long

, p. 1023 - 1026 (2012/10/08)

Ten novel 5-substituted derivatives of 3-(1-hydroxyethylidene)pyrrolidine- 2,4-dione were synthesized. The compounds were confirmed by IR, 1H NMR, MS and elemental analysis. The bioassay indicated that these compounds showed noticeable herbicid

Oleanolic acid and its derivatives: New inhibitor of protein tyrosine phosphatase 1B with cellular activities

Zhang, Yi-Nan,Zhang, Wei,Hong, Di,Shi, Lei,Shen, Qiang,Li, Jing-Ya,Li, Jia,Hu, Li-Hong

, p. 8697 - 8705 (2008/12/23)

Protein tyrosine phosphatase 1B is a key factor in the negative regulation of insulin pathway and a promising target for treatment of diabetes and obesity. Herein, a series of competitive inhibitors were optimized from oleanolic acid, a natural triterpenoid identified against PTP1B by screening libraries of traditional Chinese medicinal herbs. Modifying at 3 and 28 positions, we obtained compound 13 with a Ki of 130 nM, which exhibited good selectivity between other phosphatases involved in insulin pathway except T-cell protein tyrosine phosphatase. Further evaluation in cell models illustrated that the derivatives enhanced insulin receptor phosphorylation in CHO/hIR cells and also stimulated glucose uptake in L6 myotubes with or addition of without insulin.

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