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91990-88-4

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91990-88-4 Usage

Chemical Properties

White Crystalline Solid

Uses

Different sources of media describe the Uses of 91990-88-4 differently. You can refer to the following data:
1. A photoactivatable analog of glutathione disulfide.
2. Heterobifunctional photoreactive crosslinker. Succinimidyl ester will react with amines and the benzophenone will react non-specifically upon photoirradiation at approximately 360 nm.
3. An amine reactive heterobifunctional reagent.

Check Digit Verification of cas no

The CAS Registry Mumber 91990-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,9 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91990-88:
(7*9)+(6*1)+(5*9)+(4*9)+(3*0)+(2*8)+(1*8)=174
174 % 10 = 4
So 91990-88-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H13NO5/c20-15-10-11-16(21)19(15)24-18(23)14-8-6-13(7-9-14)17(22)12-4-2-1-3-5-12/h1-9H,10-11H2

91990-88-4 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (S0863)  N-Succinimidyl 4-Benzoylbenzoate  >98.0%(HPLC)(N)

  • 91990-88-4

  • 200mg

  • 830.00CNY

  • Detail
  • TCI America

  • (S0863)  N-Succinimidyl 4-Benzoylbenzoate  >98.0%(HPLC)(N)

  • 91990-88-4

  • 1g

  • 2,690.00CNY

  • Detail

91990-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,5-dioxopyrrolidin-1-yl) 4-benzoylbenzoate

1.2 Other means of identification

Product number -
Other names p-benzoylbenzoic acid N-hydroxysuccinimide 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:91990-88-4 SDS

91990-88-4Relevant articles and documents

High-throughput multiplexed competitive immunoassay for pollutants sensing in water

Desmet, Cloé,Blum, Loic J.,Marquette, Christophe A.

, p. 10267 - 10276 (2012)

The present study described the development and evaluation of a new fully automated multiplex competitive immunoassay enabling the simultaneous detection of five water pollutants (okadaic acid (OA), 2-chloro-4-ethylamino-6- isopropylamino-1,3,5-triazine (atrazine), 2.4-dichlorophenoxyacetic acid (2,4-D), 2,4,6-trinitrotoluene (TNT), and 1,3,5-trinitroperhydro-1,3,5-triazine (RDX)). The technology is taking advantage of an optical-clear pressure-sensitive adhesive on which biomolecules can be immobilized and that can be integrated within a classical 96-well format. The optimization of the microarray composition and cross-reaction was performed using an original approach where probe molecules (haptens) were conjugated to different carriers such as protein (bovine serum albumin or ovalbumin), amino-functionalized latex beads, or dextran polymer and arrayed at the surface of the adhesive. A total of 17 different probes were then arrayed together with controls on the adhesive surface and screened toward their specific reactivity and cross-reactivity. Once optimized, the complete setup was used for the detection of the five target molecules (less than 3 h for 96 samples). Limits of detection of 0.02, 0.01, 0.01, 100, and 0.02 μg L-1 were found for OA, atrazine, 2,4-D, TNT, and RDX, respectively. The proof of concept of the multiplex competitive detection (semiquantitative or qualitative) of the five pollutants was also demonstrated on 16 spiked samples.

POLYCYCLIC EPOXIDES AND COMPOSITIONS THEREOF WITH ANTI-CANCER ACTIVITIES

-

Paragraph 0283-0286, (2016/12/01)

The present technology provides polycyclic epoxides of Formula I, compositions comprising such expoxides and methods of using such epoxides. In particular, these compounds are useful for inhibiting cancer cell proliferation and tumor angiogenesis or treating ovarian, breast, prostate, liver, pancreatic, and colon cancers, as well as leukemia.

Synthesis and application of a photoaffinity analog of dehydroepiandrosterone (DHEA)

Olivo, Horacio F.,Perez-Hernandez, Nury,Liu, Dongmin,Iruthayanathan, Mary,O'Leary, Brianne,Homan, Laurie L.,Dillon, Joseph S.

supporting information; experimental part, p. 1153 - 1155 (2010/06/17)

We have synthesized an analog of dehydroepiandrosterone (DHEA, 1) containing both a benzophenone (BP) and a biotin (Bt) group (DHEA-BP-Bt, 8). Compound 8 was prepared by functionalization on C-17 of 1. Biocytin was reacted with 4-benzoylbenzoic acid and t

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