Welcome to LookChem.com Sign In|Join Free
  • or
2-Oxabicyclo[4.1.0]heptane, 3-methyl-4,5-bis(phenylmethoxy)-, (1R,3S,4S,5S,6S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

162332-12-9

Post Buying Request

162332-12-9 Suppliers

Recommended suppliers

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

162332-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162332-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,3,3 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 162332-12:
(8*1)+(7*6)+(6*2)+(5*3)+(4*3)+(3*2)+(2*1)+(1*2)=99
99 % 10 = 9
So 162332-12-9 is a valid CAS Registry Number.

162332-12-9SDS

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 (1R,3S,4S,5S,6S)-4,5-Bis-benzyloxy-3-methyl-2-oxa-bicyclo[4.1.0]heptane

1.2 Other means of identification

Product number -
Other names -

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:162332-12-9 SDS

162332-12-9Downstream Products

162332-12-9Relevant academic research and scientific papers

Synthesis of 1,2-Cyclopropanated Sugars from Glycals

Murali, R.,Ramana, C. V.,Nagarajan, M.

, p. 217 - 218 (1995)

Syntheses of both forms of cyclopropanated sugars from glycals by (i) Simmons-Smith reaction and (ii) dichlorocarbene addition followed by dehalogenation are described.

Synthesis and Reactions of 1,2-Cyclopropanated Sugars

Ramana,Murali,Nagarajan

, p. 7694 - 7703 (2007/10/03)

Diastereospecific cyclopropanation of glycals 1, 2, 3, 4, and 41 was carried out using either dihalocarbene addition or zinc-carbenoid addition to yield 1,2-cyclopropanated sugars. Dichloroand dibromocarbenes added stereoselectively anti to the C3/s

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 162332-12-9