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28493-86-9

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28493-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28493-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,4,9 and 3 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28493-86:
(7*2)+(6*8)+(5*4)+(4*9)+(3*3)+(2*8)+(1*6)=149
149 % 10 = 9
So 28493-86-9 is a valid CAS Registry Number.

28493-86-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-nitrophenyl) 4-(phenylmethoxycarbonylamino)butanoate

1.2 Other means of identification

Product number -
Other names 4-nitrophenyl 4-{[(benzyloxy)carbonyl]amino}butanoate

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:28493-86-9 SDS

28493-86-9Relevant articles and documents

sym-Homospermidine, a naturally occurring polyamine.

Kuttan,Radhakrishnan,Spande,Witkop

, p. 361 - 365 (1971)

-

Synthesis of functionalized glutamine- and asparagine-type peptoids-scope and limitations

Cardenal, Carmen,Vollrath, Sidonie B. L.,Schepers, Ute,Br?se, Stefan

, p. 2237 - 2248 (2013/02/23)

N-Alkylated glycine oligomers ('peptoids') can serve as potent peptidomimetic systems. Installing different functional groups can often be a challenge, and minimizes yields and purities. Here, we describe the synthesis of different amide-containing submonomers which were obtained as free bases, as well as their incorporation into peptoids. By using the free amines, the coupling results on solid support could be improved, and various functionalized peptoids were prepared. Additionally, an interesting dimerization side reaction leading to cross-linked peptoids was observed during synthesis.

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