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159751-47-0

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  • Hexanedioic acid,2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, 6-(1,1-dimethylethyl) ester,(2S)-/ LIDE PHARMA- Factory supply / Best price

    Cas No: 159751-47-0

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159751-47-0 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 159751-47-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,7,5 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 159751-47:
(8*1)+(7*5)+(6*9)+(5*7)+(4*5)+(3*1)+(2*4)+(1*7)=170
170 % 10 = 0
So 159751-47-0 is a valid CAS Registry Number.
InChI:InChI=1/C25H29NO6/c1-25(2,3)32-22(27)14-8-13-21(23(28)29)26-24(30)31-15-20-18-11-6-4-9-16(18)17-10-5-7-12-19(17)20/h4-7,9-12,20-21H,8,13-15H2,1-3H3,(H,26,30)(H,28,29)/t21-/m0/s1

159751-47-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-6-[(2-methylpropan-2-yl)oxy]-6-oxohexanoic acid

1.2 Other means of identification

Product number -
Other names (S)-2-Fmoc-aminohexanedioic acid 6-tert-butyl ester

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:159751-47-0 SDS

159751-47-0Downstream Products

159751-47-0Relevant articles and documents

Convenient access to glutamic acid side chain homologues compatible with solid phase peptide synthesis

Ryan, Shannon J.,Zhang, Yongda,Kennan, Alan J.

, p. 4765 - 4767 (2005)

(Chemical Equation Presented) Preparation of several side chain length variants of glutamic acid is achieved via olefin cross metathesis of allyl glycine derivatives. The products are suitably protected for direct use in Fmoc solid-phase peptide synthesis, as demonstrated by successful synthesis of test sequences.

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