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L-Serine, O-[(1,1-dimethylethyl)dimethylsilyl]-N-[(phenylmethoxy)carbonyl]-L-seryl- D-phenylalanyl-O-[(1,1-dimethylethyl)dimethylsilyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

184295-95-2

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184295-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 184295-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,2,9 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 184295-95:
(8*1)+(7*8)+(6*4)+(5*2)+(4*9)+(3*5)+(2*9)+(1*5)=172
172 % 10 = 2
So 184295-95-2 is a valid CAS Registry Number.

184295-95-2SDS

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 (S)-2-{(R)-2-[(S)-2-Benzyloxycarbonylamino-3-(tert-butyl-dimethyl-silanyloxy)-propionylamino]-3-phenyl-propionylamino}-3-(tert-butyl-dimethyl-silanyloxy)-propionic acid methyl ester

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:184295-95-2 SDS

184295-95-2Downstream Products

184295-95-2Relevant academic research and scientific papers

Total synthesis and assignment of configuration of lissoclinamide 7

Wipf, Peter,Fritch, Paul C.

, p. 12358 - 12367 (2007/10/03)

The first total synthesis of lissoclinamide 7, a 21-membered cyclopeptide isolated from Lissoclinum bistratum, was accomplished in 23 steps and 4.4% overall yield. The extraordinary configurational lability of the thiazoline segments was overcome by a novel strategy combining the use of the Burgess reagent for multiple simultaneous oxazoline and thiazoline formations and an efficient oxazoline → thiazoline heterocycle interconversion. In addition to the total synthesis, this work highlights the scope of alternative strategies toward Lissoclinum peptides and presents the preparation of analogues for SAR studies of the cytotoxic effects of this family of marine natural products.

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