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1225187-10-9

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1225187-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1225187-10-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,5,1,8 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1225187-10:
(9*1)+(8*2)+(7*2)+(6*5)+(5*1)+(4*8)+(3*7)+(2*1)+(1*0)=129
129 % 10 = 9
So 1225187-10-9 is a valid CAS Registry Number.

1225187-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (9H-fluoren-9-yl)methyl (S)-(6-amino-1-((4-(((benzylcarbamoyl)oxy)methyl)phenyl)amino)-1-oxohexan-2-yl)carbamate 2,2,2-trifluoroacetate

1.2 Other means of identification

Product number -
Other names -

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:1225187-10-9 SDS

1225187-10-9Relevant articles and documents

Supramolecular hydrogels for enzymatically triggered self-immolative drug delivery

Sáez, José A.,Escuder, Beatriu,Miravet, Juan F.

supporting information; experimental part, p. 2614 - 2618 (2010/05/17)

For the first time the combination of self-immolative spacers and supramolecular hydrogels has been tested in enzyme triggered drug release. Low-molecular weight drug-gelator conjugates have been prepared, which contain a gel forming lysine moiety linked to model drugs (benzylamine and phenethylamine) through a self-immolating spacer (p-aminobenzyloxycarbonyl). In the presence of trypsin the amide linkage between the gelator moiety and the spacer is hydrolyzed leading to the release of the model drug. This approach provides with distinct advantages, such as sustained release or versatility associated to the use of supramolecular hydrogels and self-immolative spacers, respectively.

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