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3508-00-7

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3508-00-7 Usage

Uses

1-Heptadecyl Bromide (cas# 3508-00-7) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 3508-00-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,0 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3508-00:
(6*3)+(5*5)+(4*0)+(3*8)+(2*0)+(1*0)=67
67 % 10 = 7
So 3508-00-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H35Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18/h2-17H2,1H3

3508-00-7 Well-known Company Product Price

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  • Aldrich

  • (17210)  1-Bromoheptadecane  ≥95.0% (GC)

  • 3508-00-7

  • 17210-5G

  • 1,676.61CNY

  • Detail

3508-00-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-BROMOHEPTADECANE

1.2 Other means of identification

Product number -
Other names Heptadecane,1-bromo

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:3508-00-7 SDS

3508-00-7Relevant articles and documents

Cristol,Firth

, p. 280 (1961)

Light-mediated deoxygenation of alcohols with a dimeric gold catalyst

McCallum, Terry,Slavko, Ekaterina,Morin, Mathieu,Barriault, Louis

supporting information, p. 81 - 85 (2015/02/18)

A new protocol for the reductive deoxygenation of primary alcohols was explored. This photo-mediated method combines a novel approach to bromination of alcohols merged with the powerful reducing capability of [Au2(dppm)2]Cl2 [dppm = 1,1-bis(diphenylphosphino)methane] as a photoredox catalyst. The highly efficient methods discussed are marked by the use of UVA light-emitting diodes, which have significantly reduced reaction times and lowered setup cost.

Synthesis of racemic and each enantiomer of 3-methylnonacosanol, a new plant growth regulator from Lowsonia inermis

Kulkarni, Bheemashankar A.,Sankaranarayanan, Sivaraman,Subbaraman, Ayalur S.,Chattopadhyay, Subrata

, p. 1571 - 1577 (2007/10/03)

An efficient synthesis of the title compound I in racemic and enantiomeric forms has been developed starting from 10-undecenoic acid. For the enantiomeric synthesis, a lipase catalyzed acylation strategy was employed to prepare the required methyl branched chiron which was subsequently derivatized to give the enantiomers of I. The plant growth regulatory (PGR) assay of I, carried out with hypocotyl cuttings of French beans (Phaseolus vulgaris L.) in Steinberg's nutrient medium revealed appreciable activity at a concentration of 2.5 ppm. The PGR activities of the compound both in racemic and enantiomeric forms were better than 1- triacontanol, the enantiomer, (S)-I being the best test candidate.

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