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2-benzyloxy-5-iodobenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

146335-32-2

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146335-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146335-32-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,3,3 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 146335-32:
(8*1)+(7*4)+(6*6)+(5*3)+(4*3)+(3*5)+(2*3)+(1*2)=122
122 % 10 = 2
So 146335-32-2 is a valid CAS Registry Number.

146335-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Benzyloxy)-5-iodobenzoic acid

1.2 Other means of identification

Product number -
Other names Benzaldehyde,5-iodo-2-(phenylmethoxy)

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:146335-32-2 SDS

146335-32-2Downstream Products

146335-32-2Relevant academic research and scientific papers

A new convergent approach to biphenomycin antibiotics

Paintner, Franz F.,G?rler, Klaus,Voelter, Wolfgang

, p. 522 - 526 (2007/10/03)

A new, convergent approach to the biaryl key intermediate of Schmidt's biphenomycin B total synthesis has been accomplished via a palladacycle complex catalyzed Stille cross-coupling of two o-tyrosine building blocks.

Total synthesis of the biphenomycins; V. Synthesis of biphenomycin A

Schmidt,Leitenberger,Griesser,Schmidt,Meyer

, p. 1248 - 1254 (2007/10/02)

The total synthesis of biphenomycin A is described. Two of the five stereogenic centres were formed by enantioselective hydrogenation of the corresponding didehydroamino acids using the rhodium-DIPAMP catalyst and the two stereogenic centres of the α-amin

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