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Fmoc-(1S,2R)-(+)-2-aminocyclohex-4-ene-carboxylicacid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1084909-67-0

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1084909-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1084909-67-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,4,9,0 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1084909-67:
(9*1)+(8*0)+(7*8)+(6*4)+(5*9)+(4*0)+(3*9)+(2*6)+(1*7)=180
180 % 10 = 0
So 1084909-67-0 is a valid CAS Registry Number.

1084909-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,6R)-6-(9H-fluoren-9-ylmethoxycarbonylamino)cyclohex-3-ene-1-c arboxylic acid

1.2 Other means of identification

Product number -
Other names (1S,6R)-TERT-BUTYL 3,8-DIAZABICYCLO[4.2.0]OCTANE-8-CARBOXYLATE

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:1084909-67-0 SDS

1084909-67-0Downstream Products

1084909-67-0Relevant academic research and scientific papers

Synthesis of β-lactams bearing functionalized side chains from a readily available precursor

Lee, Myung-Ryul,Stahl, Shannon S.,Gellman, Samuel

supporting information; experimental part, p. 5317 - 5319 (2009/06/18)

(Chemical Equation Presented) The reaction of chlorosulfonyl isocyanate (CSI) with alkenes provides β-lactams in quantity, and the products have frequently been used for ring-opening polymerization to generate nylon-3 materials. Prior uses of this approach have focused almost entirely on β-lactams with purely hydrocarbon substitutents. We show how a variety of β-lactams bearing protected polar substituents can be generated from CSI-derived building blocks.

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