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Silane, 9H-fluoren-9-yltriphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18857-36-8

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18857-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18857-36-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,5 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18857-36:
(7*1)+(6*8)+(5*8)+(4*5)+(3*7)+(2*3)+(1*6)=148
148 % 10 = 8
So 18857-36-8 is a valid CAS Registry Number.

18857-36-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 9H-fluoren-9-yl(triphenyl)silane

1.2 Other means of identification

Product number -
Other names 9-Fluorenyl-triphenyl-silan

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:18857-36-8 SDS

18857-36-8Relevant academic research and scientific papers

Unsolvated [KFl(SiPh3)]n (Fl = fluorenyl): A supramolecular chain structure assembled exclusively through K?C-π-bonding

Zaeni, Ahmad,Olbrich, Falk,Hrib, Cristian G.,Edelmann, Frank T.

, p. 1935 - 1938 (2011)

Unsolvated potassium 9-triphenylsilylfluorenide, [KFl(SiPh 3)]n (3, Fl = fluorenyl), has been prepared in 89% yield by metalation of 9-fluorenyltriphenylsilane (2) with potassium hydride in toluene/THF and structurally characterized

Amino acid protecting groups

-

, (2008/06/13)

This invention relates to compounds of the formula a compound of the formula STR1 wherein X is O, CR7 R8, S or NR9 wherein R7 and R8 are independently hydrogen, or lower alkyl, and R9 is lower alkyl; n is 0 or 1; R1 and R2 are independently hydrogen, lower alkyl, monoorganosilyl, diorganosilyl, triorganosilyl, halogen, aryl, or nitro; R3 is hydrogen, lower alkyl, monoorganosilyl, diorganosilyl, triorganosilyl, halogen, 9-fluorenylalkyl, cycloalkyl, aryl or aralkyl; R4 and R5 are independently hydrogen, lower alkyl, or aryl or one of R4 and R5 is 9-fluorenyl; R6 is H or COZ wherein Z is an amino acid, a peptide residue or a leaving group; and with the provisos that when n is 0 and R3 is hydrogen, R1 and R2 are not hydrogen, halogen or nitro; that when n is 0 and R3 is lower alkyl, R1 and R2 are not hydrogen; and that when X is O or CR7 R8 wherein R7 and R8 are H, that R1, R2, R3, R4, R5, and R6 are not all simultaneously H. The compounds of the present invention are useful in peptide synthesis as blocking or protecting groups for reactive groups. The present invention is also directed to a method of protecting a reactive group of an organic molecule during a reaction which modifies a portion of the molecule other than the protected group.

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