Welcome to LookChem.com Sign In|Join Free

CAS

  • or

34102-49-3

Post Buying Request

34102-49-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

34102-49-3 Usage

Chemical Properties

white to off-white powder or chunks

Check Digit Verification of cas no

The CAS Registry Mumber 34102-49-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,0 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34102-49:
(7*3)+(6*4)+(5*1)+(4*0)+(3*2)+(2*4)+(1*9)=73
73 % 10 = 3
So 34102-49-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO/c9-7-5-3-1-2-4-6(5)8-7/h5-6H,1-4H2,(H,8,9)/t5-,6-/m1/s1

34102-49-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Azabicyclo[4.2.0]octan-8-one, 98%

1.2 Other means of identification

Product number -
Other names cis-7,8-Diaza-bicyclo<4.2.2>dec-7-en-7-oxid

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:34102-49-3 SDS

34102-49-3Relevant articles and documents

Nylon-3 polymers that enable selective culture of endothelial cells

Liu, Runhui,Chen, Xinyu,Gellman, Samuel H.,Masters, Kristyn S.

supporting information, p. 16296 - 16299 (2013/12/04)

Substrates that selectively encourage the growth of specific cell types are valuable for the engineering of complex tissues. Some cell-selective peptides have been identified from extracellular matrix proteins; these peptides have proven useful for biomat

Access to poly-β-peptides with functionalized side chains and end groups via controlled ring-opening polymerization of β-lactams

Zhang, Jihua,Kissounko, Denis A.,Lee, Sarah E.,Gellman, Samuel H.,Stahl, Shannon S.

body text, p. 1589 - 1597 (2009/07/30)

Poly-β-peptides are attractive for biomedical applications because the backbone is similar enough to that of proteins for biocompatibility,but the backbone is sufficiently unnatural that these polymers evade pr oteolytic degradation. Prior investigations

Synthesis of 1-[2-(hydroxymethyl)cyclohexyl]pyrimidine analogues of nucleosides: A comparative study

Vina, Dolores,Santana, Lourdes,Uriarte, Eugenio,Quezada, Elias,Valencia, Laura

, p. 2517 - 2522 (2007/10/03)

The synthesis of a new series of 1,2-disubstituted carbonucleosides analogues of pyrimidine (cyclohexane derivatives) is reported. For the synthesis of the uridine analogue 5a, either construction of the base on the amino group of the amino alcohol 3 or o

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 34102-49-3