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73105-93-8

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73105-93-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73105-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,0 and 5 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73105-93:
(7*7)+(6*3)+(5*1)+(4*0)+(3*5)+(2*9)+(1*3)=108
108 % 10 = 8
So 73105-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H7N3O3S/c11-13-12-9-5-1-4-8-7(9)3-2-6-10(8)17(14,15)16/h1-6H,(H,14,15,16)

73105-93-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-azido-5-naphthalene sulfonate

1.2 Other means of identification

Product number -
Other names 1-Azido-5-naphtalene sulfonate

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:73105-93-8 SDS

73105-93-8Relevant articles and documents

Demonstration of direct binding of cIAP1 degradation-promoting bestatin analogs to BIR3 domain: Synthesis and application of fluorescent bestatin ester analogs

Sato, Shinichi,Aoyama, Hiroshi,Miyachi, Hiroyuki,Naito, Mikihiko,Hashimoto, Yuichi

scheme or table, p. 3354 - 3358 (2009/04/05)

Overexpression of cIAP1 correlates with resistance to radiotherapy and chemotherapy in various cancers. Recently, we reported that a class of bestatin ester analogs represented by MeBS (2) destabilized and promoted the degradation of cIAP1 through auto-ub

Preparation and Characterization of Photoactivable Heterobifunctional Fluorescent Reagents

Muramoto, Koji,Kamiya, Hisao

, p. 2695 - 2700 (2007/10/02)

Two new photoactivable heterobifunctional reagents, 1-azido-5-naphthalene sulfonyl chloride (ANS-Cl) and the N-hydroxysuccinimide ester of 1-azido-5-naphthalene sulfonyl aminopropionate (NHS-ANS-AP), were synthesized and characterized.The reagents were applicable to the group-directed modification of ligands.Upon exposure to ultraviolet light, non-fluorescent modified ligands generated reactive nitrene intermediates which could react with neighboring molecules to form fluorescent products.This was demonstrated by the covalent modification of bovine serum albumin with ANS-AP by photolysis.NHS-ANS-AP was used for the preparation of a photoreactive invertebrate lectin.

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