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174810-06-1

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174810-06-1 Usage

Chemical Properties

white powder

Check Digit Verification of cas no

The CAS Registry Mumber 174810-06-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,8,1 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 174810-06:
(8*1)+(7*7)+(6*4)+(5*8)+(4*1)+(3*0)+(2*0)+(1*6)=131
131 % 10 = 1
So 174810-06-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO3/c1-2-8(7-14)13-11(15)9-5-3-4-6-10(9)12(13)16/h2-6,8,14H,1,7H2/t8-/m1/s1

174810-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2R)-1-hydroxybut-3-en-2-yl]isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-N-phthalimido-3-buten-1-ol

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:174810-06-1 SDS

174810-06-1Relevant articles and documents

Chiral β - substituted - α, β - unsaturated amino alcohol compound preparation method

-

Paragraph 0122; 0123, (2017/08/31)

The invention discloses a preparation method of a chiral beta-substituted-alpha, beta-unsaturated amino alcohol compound. In the presence of a solvent and a chiral catalyst of palladium, beta-substituted alpha, beta-unsaturated carbonic ester compound (I) performs asymmetric allylic substituted reaction in nitrogen atmosphere to generate chiral beta-substituted-alpha, beta-unsaturated amino alcohol (II). The preparation method of the invention has the advantages mild conditions and simple operation, and can realize good reaction yield and enantioselectivity; therefore, the invention has good application prospect.

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