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158257-40-0

158257-40-0

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  • (3S,4S)-4-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3-hydroxy-6-methylheptanoic acid/ LIDE PHARMA- Factory supply / Best price

    Cas No: 158257-40-0

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158257-40-0 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 158257-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,2,5 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 158257-40:
(8*1)+(7*5)+(6*8)+(5*2)+(4*5)+(3*7)+(2*4)+(1*0)=150
150 % 10 = 0
So 158257-40-0 is a valid CAS Registry Number.

158257-40-0SDS

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 (3S,4S)-4-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxy-6-methylheptanoic acid

1.2 Other means of identification

Product number -
Other names (3S,4S)-N-Fmoc-4-amino-3-hydroxy-6-methylheptanoic acid

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:158257-40-0 SDS

158257-40-0Downstream Products

158257-40-0Relevant articles and documents

Pepstatin A derivatives

-

, (2009/12/04)

The invention relates to a compound having a structure according to the general formula P3-P2-P1-P1'-P2' (I), wherein residues P3, P2, P1, P1' and P2' are specifically defined and may be, e. g., certain amino acid residues. The invention further relates to the use of said compound and to a method for synthesizing a peptide.

Synthesis of Chiral Urethane N-Alkoxycarbonyl Tetramic Acids from Urethane N-Carboxyanhydrides (UNCAs)

Fehrentz, Jean-Alain,Bourdel, Elisabeth,Califano, Jean-Christophe,Chaloin, Oliveir,Devin, Chantal,et al.

, p. 1557 - 1560 (2007/10/02)

The synthesis of chiral N-protected tetramic acid derivatives which are precursors of β-hydroxy γ-amino acid under mild conditions is described.Reaction of urethane-N-carboxyanhydrides (UNCAs) with Meldrum's acid in the presence of a tertiary amine, follo

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