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1686-56-2

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1686-56-2 Usage

Definition

ChEBI: A diterpene derived from pimarane by dehydrogenation across the C(8)1C(14) and C(15)1C(16) bonds

Check Digit Verification of cas no

The CAS Registry Mumber 1686-56-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,8 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1686-56:
(6*1)+(5*6)+(4*8)+(3*6)+(2*5)+(1*6)=102
102 % 10 = 2
So 1686-56-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H32/c1-6-19(4)13-10-16-15(14-19)8-9-17-18(2,3)11-7-12-20(16,17)5/h6,14,16-17H,1,7-13H2,2-5H3/t16-,17-,19+,20+/m0/s1

1686-56-2SDS

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 pimara-8(14),15-diene

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:1686-56-2 SDS

1686-56-2Relevant articles and documents

-

Laidlaw,R.A.,Morgan,J.W.W.

, p. 644 - 650 (1963)

-

Ireland,Schiess

, p. 37,40 (1960)

Evident and latent plasticity across the rice diterpene synthase family with potential implications for the evolution of diterpenoid metabolism in the cereals

Morrone, Dana,Hillwig, Matthew L.,Mead, Matthew E.,Lowry, Luke,Fulton, D. Bruce,Peters, Reuben J.

scheme or table, p. 589 - 595 (2012/03/08)

The evolution of natural product biosynthetic pathways can be envisioned to occur via a number of mechanisms. In the present study we provide evidence that latent plasticity plays a role in such metabolic evolution. In particular, rice (Oryza sativa) produces both ent- and syn-CPP (copalyl diphosphate), which are substrates for downstream diterpene synthases. In the present paper we report that several members of this enzymatic family exhibit dual reactivity with some pairing of ent-, syn- or normal CPP stereochemistry. Evident plasticity was observed, as a previously reported ent-sandaracopimaradiene synthase also converts syn-CPP into syn-labda-8(17),12E,14-triene, which can be found in planta. Notably, normal CPP is not naturally found in rice. Thus the presence of diterpene synthases that react with this non-native metabolite reveals latent enzymatic/metabolic plasticity, providing biochemical capacity for utilization of such a novel substrate (i.e. normal CPP) which may arise during evolution, the implications of which are discussed. The Authors Journal compilation

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