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313469-03-3

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313469-03-3 Usage

General Description

10-N-Boc-amino-dec-1-ene is a chemical compound with the molecular formula C16H29NO3. It is a derivative of dec-1-ene, which is a linear alpha-olefin. 10-N-Boc-amino-dec-1-ene contains a Boc-protected amino group at the 10th position of the carbon chain. Boc is a common protecting group used in organic synthesis to temporarily mask the amino group's reactivity. 10-N-Boc-amino-dec-1-ene has potential applications in organic chemistry, pharmaceuticals, and materials science due to its specific chemical structure and reactivity. It is important to handle and use this compound with caution, following proper safety procedures and regulations.

Check Digit Verification of cas no

The CAS Registry Mumber 313469-03-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,4,6 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 313469-03:
(8*3)+(7*1)+(6*3)+(5*4)+(4*6)+(3*9)+(2*0)+(1*3)=123
123 % 10 = 3
So 313469-03-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H29NO2/c1-5-6-7-8-9-10-11-12-13-16-14(17)18-15(2,3)4/h5H,1,6-13H2,2-4H3,(H,16,17)

313469-03-3SDS

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 tert-butyl N-dec-9-enylcarbamate

1.2 Other means of identification

Product number -
Other names 10-N-Boc-amino-dec-1-ene

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:313469-03-3 SDS

313469-03-3Downstream Products

313469-03-3Relevant articles and documents

Design and synthesis of a macrosphelide A-biotin chimera

Yun, Hwayoung,Sim, Jaehoon,An, Hongchan,Lee, Jeeyeon,Lee, Hun Seok,Shin, Young Kee,Paek, Seung-Mann,Suh, Young-Ger

, p. 7127 - 7135 (2014)

The rational design and synthesis of a biochemical probe of natural (+)-macrosphelide A, a potent cell-cell adhesion inhibitor, was completed to aid in the identification of its biological target. The key features of the synthesis include: (1) an efficient synthesis of the macrosphelide core structure using Yamaguchi-Hirao alkynylation, (2) a cross metathesis to connect a linker unit to the allyl-macrosphelide and (3) coupling of the linker-bound macrosphelide A with a chemical biotin tag. This journal is the Partner Organisations 2014.

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