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N-(4-aminobenzoyloxy)succinimide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132445-64-8 Structure
  • Basic information

    1. Product Name: N-(4-aminobenzoyloxy)succinimide
    2. Synonyms: N-(4-aminobenzoyloxy)succinimide
    3. CAS NO:132445-64-8
    4. Molecular Formula: C11H10N2O4
    5. Molecular Weight: 234.21
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132445-64-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 428.7°Cat760mmHg
    3. Flash Point: 213.1°C
    4. Appearance: /
    5. Density: 1.45g/cm3
    6. Vapor Pressure: 1.48E-07mmHg at 25°C
    7. Refractive Index: 1.633
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N-(4-aminobenzoyloxy)succinimide(CAS DataBase Reference)
    11. NIST Chemistry Reference: N-(4-aminobenzoyloxy)succinimide(132445-64-8)
    12. EPA Substance Registry System: N-(4-aminobenzoyloxy)succinimide(132445-64-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 132445-64-8(Hazardous Substances Data)

132445-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132445-64-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,4,4 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132445-64:
(8*1)+(7*3)+(6*2)+(5*4)+(4*4)+(3*5)+(2*6)+(1*4)=108
108 % 10 = 8
So 132445-64-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2O4/c12-8-3-1-7(2-4-8)11(16)17-13-9(14)5-6-10(13)15/h1-4H,5-6,12H2

132445-64-8SDS

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 (2,5-dioxopyrrolidin-1-yl) 4-aminobenzoate

1.2 Other means of identification

Product number -
Other names Para-abs

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:132445-64-8 SDS

132445-64-8Relevant articles and documents

Broad-specificity immunoassays for sulfonamide detection: Immunochemical strategy for generic antibodies and competitors

Franek, Milan,Diblikova, Iva,Cernoch, Ivo,Vass, Maria,Hruska, Karel

, p. 1559 - 1567 (2006)

Development of antibodies with broad specificity recognition for sulfonamide drugs was found to be surprisingly difficult when conventional immunochemical strategies were applied to hapten design. To improve the cross-reactivity pattern of antibodies for

Pretargeting kit, method and agents used therein

-

Page/Page column 23, (2016/10/31)

Described is a pretargeting method, and related kits, for targeted medical imaging and/or therapeutics, wherein use is made of abiotic reactive chemical groups that exhibit bio-orthogonal reactivity towards each other. The invention involves the use of [4

Palladium-Catalyzed Carbonylation of (Hetero)Aryl, Alkenyl and Allyl Halides by Means of N-Hydroxysuccinimidyl Formate as CO Surrogate

Barré, Ana?s,T?nta?, Mihaela-Liliana,Alix, Florent,Gembus, Vincent,Papamica?l, Cyril,Levacher, Vincent

, p. 6537 - 6544 (2015/10/05)

An efficient Pd-catalyzed carbonylation protocol is described for the coupling of a large panel of aryl, heteroaryl, benzyl, vinyl and allyl halides 2 with the unusual N-hydroxysuccinimidyl (NHS) formate 1 as a CO surrogate to afford the corresponding valuable NHS esters 3. High conversion to the coupling products was achieved with up to 98% yield by means of Pd(OAc)2/Xantphos catalyst system.

Aniline-terminated DNA catalyzes rapid DNA-hydrazone formation at physiological pH

Domaille, Dylan W.,Cha, Jennifer N.

supporting information, p. 3831 - 3833 (2014/04/03)

We report the effect of DNA-templation on aniline-catalyzed N-acylhydrazone formation. The reaction occurs in both two-component and three-component systems. Through systematic catalyst modifications, we are able to increase the efficiency of the DNA-temp

PRETARGETING KIT, METHOD AND AGENTS USED THEREIN

-

Paragraph 0151; 0152, (2013/07/31)

Described is a pretargeting method, and related kits, for targeted medical imaging and/or therapeutics, wherein use is made of abiotic reactive chemical groups that exhibit bio-orthogonal reactivity towards each other. The invention involves the use of [4

Synthesis of chemiluminescent biotinyl naphtho[1,8-de][1,2]diazepine-1,4- diones

Krishna Murthy,Ram Reddy

, p. 2512 - 2522 (2007/10/03)

A new chemiluminescent seven numbered cyclic peri hydrazide, 6-amino-2,3-dihydronaphtho[1,8-de][1,2]diazepine-1,4-dione (AH, 4), and five of its biotin conjugates with various spacer groups are synthesized. The total framework of the chemiluminescent biot

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