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AC-ASP(OTBU)-OH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

117833-18-8

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117833-18-8 Usage

Physical Form

A crystalline solid

Uses

AC-Asp(OtBU)-OH is a useful research chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 117833-18-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,8,3 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 117833-18:
(8*1)+(7*1)+(6*7)+(5*8)+(4*3)+(3*3)+(2*1)+(1*8)=128
128 % 10 = 8
So 117833-18-8 is a valid CAS Registry Number.

117833-18-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (H63933)  N-Acetyl-L-aspartic acid 4-tert-butyl ester, 95%   

  • 117833-18-8

  • 250mg

  • 603.0CNY

  • Detail
  • Alfa Aesar

  • (H63933)  N-Acetyl-L-aspartic acid 4-tert-butyl ester, 95%   

  • 117833-18-8

  • 1g

  • 1813.0CNY

  • Detail
  • Alfa Aesar

  • (H63933)  N-Acetyl-L-aspartic acid 4-tert-butyl ester, 95%   

  • 117833-18-8

  • 5g

  • 7242.0CNY

  • Detail

117833-18-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name AC-ASP(OTBU)-OH

1.2 Other means of identification

Product number -
Other names N-Acetyl-L-aspartic acid 4-tert-butyl 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:117833-18-8 SDS

117833-18-8Downstream Products

117833-18-8Relevant articles and documents

VEGF NEUTRALIZING PRODRUGS FOR THE TREATMENT OF OCULAR CONDITIONS

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Page/Page column 146; 147, (2014/05/07)

The present invention relates to a pharmaceutical composition comprising one or more pharmaceutically acceptable excipient(s) and a VEGF neutralizing prodrug, which comprises a VEGF neutralizing biologically active moiety, for use in a method for the treatment of one or more ocular conditions.

Using peptidic inhibitors to systematically probe the S1′ site of caspase-3 and caspase-7

Goode, David R.,Sharma, Anil K.,Hergenrother, Paul J.

, p. 3529 - 3532 (2007/10/03)

(Chemical Equation Presented) Fifteen ketone-containing peptides were designed, synthesized, and used to probe the effect of substitution at the P1′ position on caspase-3 and -7 inhibition. Even with the large bias of Ac-Asp-Glu-Val-Asp at the P4-P1 positions, certain peptides with cyclic functionality in the P1′ position show a dramatically reduced ability to inhibit these caspases. Additionally, trends toward isozyme selectivity were also uncovered for particular P1′ substituents. The data indicate that substitution in the P1′ position can drastically affect both caspase inhibition and selectivity.

N-acetylaspartylglutamic acid and its β-isomer

Piotrovskii, L. B.,Dumpis, M. A.,Poznyakova, L. N.,Aleksandrova, L. N.,Sepetov, N. F.

, p. 96 - 100 (2007/10/02)

The α-isomer is predominantly formed in the synthesis of N-acetylaspartylglutamic acid and its β-isomer upon cleavage of N-acetylaspartic acid anhydride by the diethyl ester of glutamic acid.

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